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Title: Registered Nurse - Comprehensive Rehab

Location: Charlestown United States

time type

Part time

job requisition id

RQ4061666

Job Description:

Site: The Spaulding Rehabilitation Hospital Corporation

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

Job Summary

Summary

Accountable for interpreting the plan of medical care, assessment of patients' clinical decision-making regarding nursing care, assuring nursing care is provided in a safe and competent manner, providing inidualized nursing care, and evaluating nursing care for groups of patients.

Does this position require Patient Care?

Yes

Essential Functions

• Maintain accurate, detailed reports, and records.
• Administer medications to patients and monitor patients for reactions or side effects.
• Record patients' medical information and vital signs.
• Monitor, record, and report symptoms or changes in patients' conditions.
• Consult and coordinate with healthcare team members to assess, plan, implement, or evaluate patient care plans.
• Modify patient treatment plans as indicated by patients' responses and conditions.

Qualifications

Education

Associate's Degree Nursing required or Bachelor's Degree Nursing preferred

Can this role accept experience in lieu of a degree?

No

Licenses and Credentials

Registered Nurse [RN - State License] - Generic - HR Only required

Experience

Clinical nursing experience 0-1 year required

Knowledge, Skills and Abilities

• Familiarity with the principles and skills needed for practical nursing to provide patient care and treatment.
• Knowledgeable of the care required by respective age groups for which care is being provided.
• Ability to maintain confidentiality and secure sensitive information.
• Knowledge of medical terminology.
• Excellent verbal and communication skills.
• Ability to accurately screen and triage acute patients.

Additional Job Details (if applicable)

Physical Requirements

• Standing Frequently (34-66%)
• Walking Frequently (34-66%)
• Sitting Occasionally (3-33%)
• Lifting Frequently (34-66%) 35lbs+ (w/assisted device)
• Carrying Frequently (34-66%) 20lbs - 35lbs
• Pushing Occasionally (3-33%)
• Pulling Occasionally (3-33%)
• Climbing Rarely (Less than 2%)
• Balancing Frequently (34-66%)
• Stooping Occasionally (3-33%)
• Kneeling Occasionally (3-33%)
• Crouching Occasionally (3-33%)
• Crawling Rarely (Less than 2%)
• Reaching Frequently (34-66%)
• Gross Manipulation (Handling) Frequently (34-66%)
• Fine Manipulation (Fingering) Frequently (34-66%)
• Feeling Constantly (67-100%)
• Foot Use Rarely (Less than 2%)
• Vision - Far Constantly (67-100%)
• Vision - Near Constantly (67-100%)
• Talking Constantly (67-100%)
• Hearing Constantly (67-100%)

Remote Type

Onsite

Work Location

300 First Avenue

Scheduled Weekly Hours

32

Employee Type

Regular

Work Shift

Evening (United States of America)

Pay Range

$37.76 - $82.96/Hourly

Grade

SRHRN460

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

EEO Statement:

1400 The Spaulding Rehabilitation Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all iniduals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. 

Mass General Brigham Competency Framework

At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Title: Regulatory Affairs Manager

Location: USA Home Office Eastern 

Job Description:

Dentsply Sirona is the world's largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona's products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona's global headquarters is located in Charlotte, North Carolina, USA. The company's shares are listed in the United States on NASDAQ under the symbol XRAY.

Bringing out the best in people

As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we're looking for the best to join us.

Working at Dentsply Sirona you are able to:

Develop faster - with our commitment to the best professional development.

Perform better - as part of a high-performance, empowering culture.

Shape an industry - with a market leader that continues to drive innovation.

Make a difference -by helping improve oral health worldwide.

This position can be a remote working arrangement. Candidates must be located in the US, ideally in the eastern time zone.

Job Summary:

The primary job responsibility for this position is overseeing the day-to-day functions of the Dentsply Sirona Essential Dental Solutions team. This role develops regulatory strategies for existing, new, and modified medical devices and other (regulated) products. This role manages and submits 510ks for the products and manages communications with FDA including pre-subs. The inidual will also be responsible for mentoring and providing guidance to their direct reports and cross-functional product development teams on US and EU regulatory requirements.

This role works closely with business partners for registrations in their respective countries to ensure compliance globally and acts as an internal champion for initiatives aimed at improving business systems and compliance.

Key Responsibilities:

• Develops and implements regulatory strategies to obtain and maintain regulatory approvals for medical devices and other regulated products globally.
• Leads and manages regulatory submissions, including 510(k) submissions, and technical files for CE marking.
• Manages communications with FDA and EU notified bodies on behalf of the company for FDA pre submissions, FDA 510(k) submissions and EU technical files submissions.
• Provides regulatory guidance and support to cross-functional teams throughout the product lifecycle. Reviews and interprets regulatory requirements and guidance documents to ensure compliance.
• Coordinates regulatory activities with internal teams and external regulatory agencies.
• Reviews and approves product labelling and claims for the US and EU markets.
• Stays current with regulatory requirements and updates affected policies and procedures.
• Fosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationships.
• Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching, performance reviews, developmental plans, succession planning.
• Complies with company and departmental policies and administrative requirements.
• Performs other duties as assigned or as needed.

Education:

• Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline.
• Regulatory Certification (such as RAC from the Regulatory Affairs Professionals Society) or Master's degree in a scientific discipline is a plus.

Years and Type of Experience:

• 5(+) years of experience in regulatory affairs, preferably in the medical device industry.
• Experience with leading regulatory submissions and managing regulatory projects.
• In-depth knowledge of FDA 510(k) and international regulations (e.g., EN ISO 13485, EU MDR).
• Experience with software as a medical device, AI and/or medical devices containing software is a plus

Required Computer / Software Skills:

• Proficiency with Microsoft Office Suite
• Proficiency with Regulatory software

Key Required Skills, Knowledge, and Capabilities:

• Strong leadership, project management, and organizational skills including attention to detail.
• Strong written and verbal communication skills.
• Prior technical writing experience and proven track record with FDA and EU regulatory submissions.
• Excellent interpersonal skills.
• Ability to work effectively in a team environment and independently.
• Knowledge of regulatory affairs principles and practices.
• Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly, and conclusions are adequately supported.
• Willingness to learn and adapt to new processes and technologies.
• Leadership experience within medical device organizations.

Key Leadership Behaviors:

• Actively articulates and promotes Dentsply Sirona's vision and direction.
• Advocates on behalf of the customer.
• Values driven with an insistence on excellence.
• Promotes high performance, innovation, and continual improvement.
• Consistently meets Company standards, ethics, and compliance requirements.
• Strong results orientation and analytical skills.
• Clear and effective communication with key stakeholders, which span across multiple levels, socio-geographic areas, and functional expertise.
• Resolves conflicts and fosters a positive working environment.

Dentsply Sirona is an Equal Opportunity/ Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona.

Title: Collector, Drug & Alcohol Testing - Mobile - Raleigh NC

Location: Browns Summit United States

remote

Category Per Diem and On Call

Job Description:

Category Per Diem and On Call Location Browns Summit, North Carolina Job function Operations Job family Per Diem Examiner

Shift Day Employee type On-Call Work mode Remote

Job Description

The Mobile Collector, Drug & Alcohol is responsible for the successful collection of specimens according to established procedures using DOT/Non DOT guidelines. Completes random and emergency observed urine collections of same sex clients as needed. Collects specimens for drug screenings and other Quest Diagnostics services.

This is an on-call position, there is not a minimum or maximum amount of hours guaranteed or scheduled. Collector is able to accept work orders as needed and as schedule allows.

Responsibilities:

• All collectors are responsible for completing Chain of Custody (COC) forms and Alcohol Testing Forms accurately. Ensure appropriate forms are utilized based on collection type, label specimens and return via completed forms within 24 hours of collection.
• Responsible for the safe and timely transporting of specimens, supplies, equipment and materials to the appropriate destination.
• Maintain all appropriate collections logs, complete accuracy checks and monthly calibrations, maintain or complete DOT and BAT certifications.
• Works effectively with staff employees to ensure compliance with dress code, EHS & QA requirements, customer service requirements and SOP's, advising Manager or Supervisor of any issues or problems as they arise.
• Works independently to manage schedule on an as needed basis.

Qualifications:

Required Work Experience:

• DOT and NON -DOT Urine Certification - NDASA or SAPPA Certifications preferred.
• BAT certification
• Mock completion documentation
• Must have valid driver's license and clean driving record with access to dependable and insured transportation.
• Computer, internet, cell phone, printer & scanner required.
• Flexible travel (up to 100-mile radius) and flexible work hours. Maintain dates of availability and dates unavailable as appropriate.

Preferred Work Experience:

• Background in collection services and/or BAT/Urine collection preferred.
• Phlebotomy background preferred

Physical Requirements:

• Must have valid driver's license and clean driving record with access to dependable and insured transportation.
• Computer, internet, cell phone, printer & scanner required.
• Flexible travel (up to 100-mile radius) and flexible work hours. Maintain dates of availability and dates unavailable as appropriate.
• Routinely lift up to 25 pounds.
• Standing for long periods of time

Skills:

• Effective written and verbal communication skills
• Ability to keep accurate inventory of necessary supplies, provided by WHS, on hand.
• Ensures equipment is neat, clean and in good repair.
• Fine attention to detail is required

Travel Required

English Required

Education:

• High school graduate or equivalent (Preferred)
• BAT DOT certification (Preferred)
• DOT UA certification (Preferred)
• NON-DOT Certification (Preferred)

58929

Quest Diagnostics honors our service members and encourages veterans to apply.

While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any inidual as to whom an agency has sent an unsolicited resume.

Title: Test Fixture Designer - The Toro Company

Location: Bloomington United States

Full time

job requisition id

JR15993

We are unable to sponsor or take over sponsorship of a school/employment or any other visa , regardless of expiration date, now or in the future. Applicants must be legally authorized to work in the United States

Who Are We?     

The Toro Company is a homegrown, Minnesota-based company that has been in business since 1914. We pride ourselves on providing world class equipment to help maintain the environment that we love, while putting an emphasis on giving back to the communities that surround us. From residential lawns and gardens to venues such as St. Andrews Links and Target Field, we are a company with a global footprint and a passion for helping people beautify whatever landscape they may be in. With 100 years of operation under our belt and an average employee tenure of 15 years, come find out what makes The Toro Company the best place in the Twin Cities to build a career. 

This position is responsible for fixture designs related to their use within the Product Evaluation/Test Department.  Has responsibilities to the Engineering and Management group on effective fixture design to evaluate prototype and production products and components.

What Will You Do?  

In order to grow and build a successful career with The Toro Company, you will be responsible for:  

• Design of lab fixtures including, but not limited to: roll-drum dynamometers, component loading fixtures, component holding for static environmental evaluations, machine safety test apparatus, and accelerated life fixtures.

• Prepare fixture design layouts and coordinate designs with others assigned to the project to ensure integration of the design.

• Responsible for basic design calculations such as gear pulley ratios, MPH, rpm's, and weight distribution.

• Secure assistance of consultants or internal specialists i.e. CAE analysis support engineers, manufacturing engineers, and/or vendor experts.

• Use the best technology available in each and every area of design.

• Assure that all parts designed can be manufactured.

• Maintain accurate lists of parts created. Coordinate, or help to coordinate, the release of parts for fixture assembly.

• Work with design engineers and test engineers and others to incorporate product design under test into fixture, including updates to product design as it evolves during development. Solve design problems. Coordinate the required documentation to assure that the changes are implemented on a timely basis.

• CAD/CREO utilized as necessary to do project related work.

• Keep supervisor informed of project status and issues that may require assistance.

• Keep informed of new design, manufacturing and materials developments.

• Perform miscellaneous duties as may be requested

What Do You Need?  

To be considered for this role, an inidual should meet the following minimal requirements:  

• Graduate of accredited technical school for machine design and drafting (two-year course) combined with entry level design experience (zero to two years) in the mechanical drafting or design field -OR-

• Graduate of an accredited university or college with a Bachelor of Science degree in an engineering related technology (ex. Automotive, Manufacturing, Design.) 

• 1+ year(s) of experience in the mechanical drafting field

• Demonstrated design capability.

• Knowledge of force, torque, speed, acceleration, and similar mechanical calculations, troubleshooting test fixture operations, knowledge of fabrication processes including:  sheet metal bending, welding, machining (mill, lathe, and multi-axis), fastener selection, casting, painting, etc.

• Basic knowledge and understanding of general fixture design

• Basic knowledge of Data Acquisition tools, e.g. multi-meter, gauges, thermistors/thermocouples, etc.

• Demonstrates the ability to identify and sort out relevant information

• Basic knowledge of regulatory standards and requirements for mobile machinery

• Able to work independently with minimum supervision

• Travel to test sites

What Can We Give You?     

At The Toro Company, we are always working to make sure our employees know just how valued they are. In addition to a competitive salary, an affordable and top tier medical/dental/vision plan, 401k, and many other great benefits - The Toro company offers employees at our Bloomington, MN HQ location a variety of perks, including:  

Dress for your day - We know you're more productive when you're comfortable, which is why TTC employees are encouraged to take advantage of our casual, corporate environment.  

Location – Conveniently located near both St. Paul and Minneapolis, we are centrally located for most commuters!  

Food - Take advantage of our onsite café, which serves both breakfast and lunch. With a Caribou Coffee attached, you can grab a snack and a coffee at any time during your day.  

Wellness - The Toro Company’s HQ offers complimentary use of our onsite fitness facility to employees. In addition to physical wellbeing, TTC offers a variety of mental health and financial health resources to all employees.  

Volunteerism - The Toro Company is proud to provide employees 20 hours of paid time to volunteer in the community.  

Summer Hours – Enjoy a flexible schedule during the summer! By working a little more during the first few days of the week, TTC employees at our Bloomington HQ are able to start their weekends early and leave by noon on Friday.  

Flexible Work Arrangements – This team is currently implementing a hybrid work schedule. The opportunity to collaborate in the office and work from home part-time, has promoted team-building and flexibility. 

Competitive Salary – The pay range takes into account skills, experience, education, and location. It is not common to be hired at or near the top of the range; compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the annual pay range is between ​$63600 - ​$80000. Cash compensation is one piece of our competitive total rewards package. You may be eligible to participate in an incentive program, which rewards employees based on inidual and organizational performance. Eligibility and award amounts are determined by company policy and performance metrics. 

The Toro Company is an Equal Opportunity Employer. We consider all qualified applicants based on merit and do not discriminate on the basis of race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, military service, or other non-merit factors. We are committed to creating a welcoming environment for all employees

Title: RN - Carle Direct

Location: Urbana, Illinois

Work Type: Remote

Job Description:

(external candidates only)

• Requires approximately 10 weeks of in office training (Urbana, IL) with the potential to be remote after that time period*

The Transfer Center RN Specialist is dedicated to facilitating appropriate patient transfers into Carle Hospital from referring physicians and facilities (hospitals, clinics, etc.). Obtains appropriate patient information critical to determining the appropriate Carle provider, medical necessity and level of care, and demographic information. Responsible for facilitating a conference call between the referring physician and the Carle receiving physician, and will ensure, when appropriate, that an appropriate level of care bed within Carle is identified, and facilitate a timely mode of transportation. Responsible for meeting the needs and expectations of referring physicians/facilities, as well as accepting physicians by supporting and managing the patient transport process efficiently and effectively. Efficiently engages appropriate departments in the transfer process and monitors and documents all activities associated with the transfer. Responsible for oversight of the entire transfer episode, from start to finish, for communication back to the referring facility, and for communication to the physicians assuming care of the patient post-discharge from Carle.

Qualifications

Certifications: Licensed Registered Professional Nurse (RN) - Illinois Department of Financial and Professional Regulation (IDFPR)Illinois Department of Financial and Professional Regulation (IDFPR)Illinois Department of Financial and Professional Regulation (IDFPR)

Education: College Nursing diploma

Work Experience: EMR 1+ years

Responsibilities

Expedites consultation between referring patient-care providers and receiving physicians.Demonstrates strong clinical assessment skills to appropriately assess patient acuity and needs, assumes principal responsibility for the coordination of acceptance, admission and transfer, and necessary communication between the referring physician, attending physician and clinical staff.Utilizes established scripts and algorithms to facilitate smooth transition into Carle Hospital.Develop high quality professional relationships with providers and staff at referring facilities to ensure that transfers are timely and appropriate with high level patient care while ensuring maximum patient safety, optimal physician and consumer satisfaction while promoting Carle Service Line to existing and potential network hospitals. This will include site visits with referral sources to better understand their needs.In collaboration with House Officers/Throughput Officers maximize organizational patient flow and capacity management. Communicate patient placement needs utilizing contemporary guidelines and principles of patient safety, clinical relevance, patient care, patient acuity and nursing care requirements and corresponding workload ramifications.Conducts recorded three-way calls between referring physician and facility physician as well as nurse-to-nurse report.Ensures documentation is concise, meets standards utilizing all appropriate forms, and is completed in a timely, accurate manner.In addition to facilitating communication prior to and during the transfer process, the nurse in this role will be responsible for maintaining communication after the patient stay in order to maintain continuity of care for the referred patient. Provides follow-up calls and communication with both internal and external customers to meet the needs of the patient.When necessary, facilitate transfer to other appropriate facilities if Carle Hospital is unable to provide the services required to accommodate patient needs.

About Us

Find it here.

Discover the job, the career, the purpose you were meant for. At Carle Health, we're committed to fostering a workplace where every team member feels valued, respected and empowered, where passion and purpose come together to positively impact the lives of our patients and our communities. Find it all at Carle Health.

Our nearly 17,000 team members and providers work together to support patient care across central and southeastern Illinois. We've grown to include eight, award-winning hospitals and a multispecialty provider group with more than 1,500 doctors and advanced practice providers. We're developing the next generation of providers and healthcare professionals through Carle Illinois College of Medicine, the world's first engineering-based medical school, and Methodist College. Carle BroMenn Medical Center, Carle Foundation Hospital, Carle Health Methodist Hospital, Carle Health Proctor Hospital, Carle Health Pekin Hospital, and Carle Hoopeston Regional Health Center hold Magnet designations, the nation's highest honor for nursing care. We offer opportunities in several communities throughout central Illinois with potential for growth and life-long careers at Carle Health.

Compensation and Benefits

The compensation range for this position is $30.39per hour - $52.27per hour. This represents a good faith minimum and maximum range for the role at the time of posting by Carle Health. The actual compensation offered a candidate will be dependent on a variety of factors including, but not limited to, the candidate's experience, qualifications, location, training, licenses, shifts worked and compensation model. Carle Health offers a comprehensive benefits package for team members and providers

Title: Territory Sales Specialist - Wound Care

San Francisco, CA

San Jose, CA, USA

Job Description:

Essity is a global leader in health and hygiene with our corporate headquarters in Stockholm, Sweden, and North American headquarters in Philadelphia, PA. We are a multi-billion-dollar company that is committed to breaking barriers to well-being. Essity does this through innovative brands in the areas of Professional Hygiene, Consumer Goods, and Health & Medical Solutions.

Working at Essity is not just a career; it is a chance to directly make the world a healthier, more hygienic and safer place. With impactful innovations coupled with sustainable solutions, we strive to reach more people every year with the necessary and essential solutions for well-being. At Essity you will find a caring and compassionate culture where we remain grounded in our beliefs & behaviors.

About the Role

Essity is looking for an experienced Territory Sales Specialist - Wound Care. Responsible for managing and increasing the Essity Advanced Wound Care product portfolio sales within the assigned geographic territory. The product portfolio contains clinically unique brands such as Hydrofera Blue, Cutimed -Sorbact, Sorbion, and Epiona, Hypafix, and Jobst - Compri2 and Comprifore. Reporting to the Regional Sales Manager, this role is the primary driver of sales within a territory or strategic metropolitan areas.  The Wound Care Specialist role is performance driven and will target multiple call points throughout the continuum of care with a primary focus on Acute Care, Surgical Areas, and Wound Care Centers as well as managing and penetrating the alternate sites of care.

This will be a remote position responsible for covering the greater San Francisco Bay area. The ideal candidate should live in the San Francisco area or in the aligned Essity Regional structure and ability to travel often.

We’re looking for people who embody our values, aren’t afraid to challenge, innovate, experiment, and move at a fast pace. We’re always looking for ways to improve our products and ourselves. If this is you, we’d love to talk. 

What You Will Do

• To meet or exceed sales targets which will be driven by key account closes and competitive conversions in all areas of the healthcare market

• To possess and effectively communicate/utilize clinical and product knowledge clearly and concisely

• Effective customer needs assessment and solution development

• Effective relationship management with key stakeholders within targeted accounts

• The ability to interact with advanced practice clinicians (Surgeons, Physician Assistants, Nurse Practitioners, WOCN's, and Nurses) and shape product choice decisions

• Effective sales process execution

• Contract implementation and effective penetration of key GPO and IDN awards

• To maintain and increase penetration in existing accounts and healthcare systems

• Effectively coordinate opportunities internally and externally with customers

• Effective territory and account planning (pre and post call planning), targeting

• To complete all administrative duties accurately and timely

Who You Are

• Bachelor's degree required

• At least 3 years of outside sales experience required; outside sales experience in the Healthcare Industry preferred.  Exposure to wound care, surgical markets a plus.

• Additional experience in Business to Business sales helpful

• Self-Motivated, Able to be work independently, Competitive, Tenacious, High Integrity, Fearless, Strategic, Passionate, and a Team Player.

• Overnight travel, work weekends, and into the evening may be applicable (approximately 25-35% of time)

• Must be fluent in Microsoft programs; Excel, Power Point, etc.

• Experience with CRM recommended (i.e. Salesforce.com. Dynamics)

What We Can Offer You

At Essity, we believe every career is as unique as the inidual and empower employees to reach their full potential in a winning culture motivated by a powerful purpose.

Compensation and Benefits

$70,000 - $85,000/annual salary range + sales incentive + benefits

Pay offered may vary depending on multiple inidualized factors such as knowledge, skills, and experience.

Along with competitive pay you will be eligible for the following benefits:

• United Healthcare PPO / EyeMed Vision Insurance / Delta Dental Insurance

• Wellness program provided through Rally

• Healthcare and Dependent Care Flexible Spending Accounts (FSA)

• 401(k) with employer match and annual employer base contribution

• Company paid Basic Life, AD&D, short-term and long-term disability insurance

• Employee Assistance Program

• PTO offering with Paid Holidays

• Voluntary benefits to include: critical illness, hospital indemnity, and accident insurance

• Employee discounts program

• Scholarship program for children of Essity employees.

Collaborative and Caring Culture | Empowerment & Engaged People | Work with Impact and A Powerful Purpose | Inidual Learning & Career Growth | Health & Safety Priority | Sustainable Value Together| Innovation| Sustainable Working Life | Total Reward

Additional Information

The Company is committed to equal employment opportunity and providing reasonable accommodations to qualified candidates and employees pursuant to applicable law. We value and encourage ersity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, military and veteran status, gender identity or expression, genetic information, or any other characteristic protected by federal, state, or local law.

Title: Billing Collection Representative

Location: Akron United States

Job Description:

Full-time, 40 hours/week

Monday-Friday 8am-4:30pm

Remote (prefer candidates that live within commutable distance from Akron, Ohio)

Summary:

The Billing Collections Rep is responsible for resolving unpaid insurance accounts, by contacting insurance companies through various means to solicit payment for applicable patient encounters.

Responsibilities:

• Develops positive relationships with payer representatives in order to collect accounts timely.

• Investigates pended claims to determine why claims were pended and resolve reasons for the pended scenario.

• Identifies and resolves trends with pended claims, which includes appeals for untimely claim submission and resolving provider credentialing issues.

• Accurately posts resolutions to accounts including updating and billing insurance and correct and repost.

• Establishes and maintains provider manuals for assigned insurance carriers and subsequent plans.

• Monitors physician's enrollment to not exceed timely filing requirements.

• Other duties as required.

Other information:

Technical Expertise

• Experience in processing and billing physician claims is required.
• Experience in the technical aspects of billing and collections required. This includes CPT and ICD coding knowledge, understanding payer remittance coding/process and outcomes analysis/reporting.
• Experience working with applicable management team members and clinic staff required.
• Proficiency is the management of CMS formatted claims required.
• Proficiency in MS Office [Outlook, Excel, Word]. Epic experience is preferred.

Education and Experience

• Education: High school diploma or equivalent is required. Bachelor's Degree is preferred.
• Certification: Medical Billing Certificate is preferred.
• Years of relevant experience: Minimum 1 year experience required. 5 years relevant experience preferred.
• Years of experience supervising: None.

Full Time

FTE: 1.000000

Status: Remote

Title: Senior Health Services Researcher- Remote

Location: Remote United States

Full time

Job Description:

Job Description Summary:

Job Description:

The Senior Health Services Researcher is a senior-level researcher responsible for leading rigorous, and policy- and practice-relevant health services research using real-world data, including electronic medical records (EMR/EHR), claims, and workforce data. The role requires strong grounding in biostatistics and epidemiology to ensure rigorous study design, valid inference, and high-quality analysis of real-world clinical data.

This inidual will serve as a hands-on analyst and methodological leader, designing and executing advanced quantitative studies that inform primary care delivery, workforce development, and health outcomes in community-based settings, particularly Federally Qualified Health Centers (FQHCs). The role emphasizes applied, implementation-oriented, and health services research that understands clinical systems and outcomes.

ROLE AND RESPONSIBILITIES

Methodological Leadership and Data Analysis

• Independently lead at least one complex multi-year research and evaluation project.
• Lead the design and execution of advanced quantitative and mixed-methods studies using EMR/EHR, claims, and other real-world data sources
• Apply rigorous methods such as causal inference, longitudinal analysis, multilevel modeling, quasi-experimental designs, and machine learning
• Serve as a hands-on analyst, directly working with large, complex datasets
• Independently design studies grounded in epidemiologic principles and execute analyses that meet peer-reviewed publication standards

EMR/EHR & Real-World Data Expertise

• Extract, clean, and analyze structured and unstructured data from electronic medical records
• Partner with clinical and IT teams to understand data architecture, workflows, and data quality limitations for analytical purposes
• Use EMR data to evaluate care delivery, patient outcomes, and quality improvement initiatives

Research & Implementation Science

• Lead and contribute to implementation and evaluation studies focused on:

• Primary care delivery models

• Care coordination and team-based care

• Workforce development and career pathways

• Cancer screening and chronic disease management

• Translate findings into actionable recommendations for health centers and partners

Funding & Scholarly Leadership

• Work closely with multidisciplinary teams including clinicians, data scientists, educators, and external partners
• Lead or contribute to grant development (federal, foundation, industry)
• Serve as Principal Investigator or Co-Investigator on funded projects
• Publish in peer-reviewed journals and present findings to national audiences

Staff Leadership & Capacity Building

• Supervise and mentor Research Scientists, and Research Associates.
• Provide high-level scientific review and methodological consultation across teams.
• Develop junior investigators toward increasing independence and funding success.
• Lead internal learning sessions to strengthen analytic and writing capacity.
• Contribute to recruitment and talent development within the research team.
• Contribute to building a strong, methodologically rigorous research culture.

External Engagement & Institutional Representation

• Serve as scientific contact for major funders and national collaborators.
• Represent Weitzman Institute in national advisory and research networks.
• Strengthen relationships with federal agencies (e.g., HRSA, NIH, CDC), foundations, academic institutions, and corporate partners.
• Ensure compliance with complex reporting requirements and performance metrics.

QUALIFICATIONS

Required Education

• Doctoral degree (PhD, ScD, DrPH, or equivalent) in public health, epidemiology, health services research, health policy, implementation science, or related field

OR

• Masters degree with at least 7 years of research experience commensurate with other requirements.

Required Experience

• Minimum 3 years of progressively responsible research experience.
• Sustained peer-reviewed publication record with evidence of scholarly impact.
• Demonstrated experience working with electronic medical record (EMR/EHR) data
• Strong track record of hands-on data analysis using large, complex datasets
• Experience working in or with primary care settings, preferably FQHCs or safety-net systems

Required Skills

• Strong foundation in biostatistics and epidemiology, including study design, bias, confounding, and causal inference
• Advanced proficiency in statistical software (Python, SAS, Stata, R, or equivalent)
• Demonstrated ability to apply statistical and epidemiologic methods to real-world healthcare data, including EMR/EHR and claims
• Experience with:
• Data cleaning and transformation of EMR/EHR data
• Statistical modeling and causal inference methods
• Machine learning and/or natural language processing (preferred)
• Familiarity with healthcare data standards (e.g., ICD, CPT, LOINC)

Preferred Qualifications

• Established professional network in primary care or health services research.
• Experience integrating innovative analytic approaches (e.g., data science, AI-enabled methods).
• Experience contributing to and leading grant proposals

PHYSICAL REQUIREMENTS/WORK ENVIRONMENT

Remote with occasional travel to healthcare sites, meetings, and conferences

Confidentiality of Information

Confidentiality of business information is a requirement. Confidentiality must be maintained according to CHC policies

This Position is available for remote work.

Time Type:

Full time

Title: Enablement Officer

Location: Enfield 

Reference Number: PEO-002578

Salary: Scale 5 £32,535 - £34,998

Department: People

Location: Park Avenue Day Centre

Contract type: Permanent

Division: People Department

Hours Per Week: 32

Contract End Date: Not specified

Interview Date: Not specified

Job Description

THE MENTAL HEALTH ENABLEMENT SERVICE Which is based at Bush Hill Park, Enfield has a vacancy for a MENTAL HEALTH ENABLEMENT OFFICER

Enfield Council’s Mental Health Enablement Service works closely with people who have severe and enduring mental health support needs in order to improve their ability to live independently and participate in the community, as well as improve quality of life and well-being.

Working mainly 1:1 in people’s homes and in the community, we provide short-term intensive support to achieve a range of agreed and personalised outcomes. Our work includes resettlement and outreach work, and support to access opportunities in employment, education and leisure. Another part of the Enablement Service is the Drop In, which offers advice, information, advocacy and support, and community links.

The successful candidate will work as part of a team, and induction, supervision and training will be available.

Contact Details -

If you would like to know more about the role, please contact [email protected] for an informal discussion or to arrange a visit to the team.

If you have any difficulties accessing this information, please contact [email protected] Recruitment & Onboarding Advisor.

“This authority is committed to safeguarding and promoting the welfare of children and young people and expects all staff and volunteers to share in this commitment”.

We reserve the right to close this vacancy once a sufficient number of applications have been received. Therefore, we advise that you complete fully and submit your application as soon as possible to avoid disappointment.

Why it's great to work for Enfield Council:

• An excellent pension through the Local Government Pension Scheme (LGPS).
• Up to 31 days annual leave depending on grade and length of service. You will also get eight public holidays per year and an extra day off at Christmas.
• A blend of remote and office based working for most roles.
• Interest free season ticket loan repayable over three or ten months.
• Career development and learning experiences from a range of training courses and learning methods.
• Employee Assistance Programme to provide advice and counselling services. This is a free and confidential service available to staff and members of their family.
• Health and leisure discounts and tax-free bikes for work.

We are passionate about our people and how we deliver services to our community in Enfield. That’s why we encourage a culture that puts our customers at the heart of everything we do - by empowering our people to work together to find solutions, be open, honest and respectful, take responsibility and listen and learn. If you value these behaviours too, we’d love to hear from you - and of course we are always happy to talk flexible working, click here to find out more.

If you have previously applied for this role within the past 6 months, unfortunately, a second application will not be considered.

We do not see your name or title when shortlisting your application. This is one of many initiatives to build a more talented and erse workforce. However, if you put your name on your CV or Statement it will be visible to us. For this reason, we ask that you do not include your name on these documents.

Please note it is your responses to the Essential/Desirable criteria that will determine if you are shortlisted for an interview, therefore we encourage you to always address the essential and desirable criteria (found in the Person Specification) in your Supporting Statement.

Title: HSS Coordinator - Remote in VA Market

Location:

Remote, VA

Job Description:

At UnitedHealthcare, we're simplifying the health care experience, creating healthier communities and removing barriers to quality care. The work you do here impacts the lives of millions of people for the better. Come build the health care system of tomorrow, making it more responsive, affordable and equitable. Ready to make a difference? Join us to start Caring. Connecting. Growing together.

The Care Coordinator will be the primary care manager for a panel of intellectually disabled/developmentally delayed members with low-to-high complexity medical/behavioral needs. Care coordination activities will focus on supporting member's medical, behavioral, and socioeconomic needs to promote appropriate utilization of services and improved quality of care.

For consideration, you must reside in the State of VA.

If you reside within the state of VA, you will have the flexibility to work remotely. However, you will need access reliable transportation as this role may require occasional field work to meet face-to-face with our members.

Primary Responsibilities:

• Engage members telephonically to complete a comprehensive needs assessment, including assessment of medical, behavioral, functional, cultural, and socioeconomic needs
• Develop and implement person centered care plans to address needs including management of chronic health conditions, health promotion and wellness, social determinants of health, medication management and member safety in alignment with evidence-based guidelines
• Partner and collaborate with internal care team, providers, and community resources/partners to implement care plan
• Provide education and coaching to support member self-management of care needs and lifestyle changes to promote health
• Support proactive discharge planning and manage/coordinate Care Transition following ER visit, inpatient or Skilled Nursing Facility (SNF) admission
• Advocate for members and families as needed to ensure the member's needs and choices are fully represented and supported by the health care team

You'll be rewarded and recognized for your performance in an environment that will challenge you and give you clear directions on what it takes to succeed in your role as well as provide development for other roles you may be interested in.

Required Qualifications:

• Bachelor's degree in health or human services Field OR LMHP OR RN/LPN OR QMHP OR LMSW OR LBSW OR MSW OR BSW
• 1+ years of care coordination or behavioral health experience and/or work in a healthcare environment
• 1+ years of experience with MS Office, including Word, Excel, and Outlook
• Experience working with members who have medical needs, intellectual disabilities, developmental delays, or iniduals with physical disabilities and/or those who may have communication barriers
• Driver's license and access to reliable transportation and the ability to travel within assigned territory to meet with members and providers
• Reside in Virginia

Preferred Qualifications:

• CCM certification
• QIDP
• Experience working with Medicaid/Medicare population
• Long term care/geriatric experience
• Experience working in team-based care
• Background in Managed Care

Pay is based on several factors including but not limited to local labor markets, education, work experience, certifications, etc. In addition to your salary, we offer benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). No matter where or when you begin a career with us, you'll find a far-reaching choice of benefits and incentives. The hourly pay for this role will range from $23.89 to $42.69 per hour based on full-time employment. We comply with all minimum wage laws as applicable.

At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone-of every race, gender, sexuality, age, location and income-deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission.

UnitedHealth Group is an Equal Employment Opportunity employer under applicable law and qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

UnitedHealth Group is a drug - free workplace. Candidates are required to pass a drug test before beginning employment.

Principal Systems Engineer

Location: Valencia, CA, US, 91355

Work mode:  Hybrid

Department: Research & Development

Job Description:

Additional Location(s): US-CA-Valencia

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of erse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.           

About the role:

Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work.

As a Principal Systems Engineer on the Boston Scientific Neuromodulation R&D team, you will play a critical role in the design and development of complex medical systems from concept through product launch. This includes wearable, implantable, and connected cloud and mobile solutions that improve patient outcomes.

In this role, you will lead system-level design efforts by translating user needs and stakeholder inputs into robust system requirements and architecture. You will guide cross-functional teams through implementation, integration, and verification activities across hardware, firmware, and software. This position requires strong technical leadership, systems thinking, and the ability to drive innovation in a highly regulated environment.

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week.

Your responsibilities will include:

• Provide technical leadership across cross-functional engineering teams to deliver complex system solutions.
• Define, analyze, and manage system requirements, including clinical workflows, patient interactions, and input/output processes using systems engineering principles.
• Develop and document system architecture using industry-standard tools to model system interactions and dependencies.
• Apply critical thinking to identify and resolve system integration challenges, providing clear recommendations and solutions.
• Create and maintain design documentation, including requirements rationale, traceability, and system change analyses within the quality system.
• Partner with internal regulatory teams to develop reports and documentation supporting external regulatory submissions.
• Apply project management principles to plan, execute, track, and communicate progress across projects of varying scope and complexity.
• Support system risk management activities, including FMEA and hazard analysis, ensuring compliance with applicable standards.

Required qualifications:

• Bachelor’s degree in biomedical engineering, electrical engineering, computer engineering, computer science, or a related field.
• Minimum of 12 years' experience in engineering; a master’s degree may substitute for 2 years of experience.
• Minimum of 10 years' experience working with mixed hardware and/or software systems.
• Minimum of 10 years' experience in the design, development, and testing in a regulated industry (medical systems and devices preferred).
• Demonstrated ability to develop and interpret system requirements and specifications.

Preferred qualifications:

• Direct experience with therapy programming and delivery, patient alerts, and usability in wearable medical devices.
• Experience with neurostimulators and neuromodulation technologies.
• Experience working in an acquisition or integration environment.
• Familiarity with ecosystems involving wearable devices, mobile applications, and patient-facing user interfaces (UI/UX).
• Proven ability to work independently with a solution-oriented mindset.
• Experience with system development lifecycle processes, including formalized procedures and documentation standards.
• Ability to interpret and apply regulations and standards relevant to Class II and Class III medical devices.
• Experience with requirements management and PLM tools.
• Experience in product concept development, customer engagement, verification, and validation activities.
• Strong written and verbal communication skills, with sound judgment and critical thinking abilities.
• Ability to build relationships across teams and with external stakeholders.
• Demonstrated technical leadership within cross-functional environments.
• Working knowledge of project management principles and exposure to Agile methodologies.
• PMP certification.

Minimum Salary: $ 102100 

Maximum Salary: $ 194000 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an inidual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

Title: Senior Regulatory Affairs Specialist

Location: Marlborough, MA, US, 01752

Department: Legal and Regulatory

Job Description:

Additional Location(s): US-CA-Irvine; US-MN-Arden Hills; US-MN-Maple Grove

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of erse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.       

About this role: 

We are looking to hire an enthusiastic inidual for a Senior Regulatory Affairs Specialist position (hybrid work mode) supporting our rapidly growing active implantable device portfolio. This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies. The role requires strong US, EU, and international regulatory experience that can be leveraged to help support international expansion. In this role, you’ll be part of a high-functioning, close-knit Regulatory Affairs team responsible for support of submissions and on-going regulatory compliance through partnership with our global R&D, manufacturing, clinical, and quality teams.

Your responsibilities will include:

• Reviews change notifications and performs regulatory impact assessment for product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings, and supports associated global submissions as needed  
• Supports the coordination, drafting, and submitting of U.S. and EU regulatory filings for new and modified Class III products   
• Provides technical reviews of test protocols and reports  
• Assesses labeling materials, including Instructions for Use  
• Represents RA on cross functional project teams 
• Works as liaison with International BSC Regulatory colleagues on various projects, including providing support with international regulatory filings 
• Supports highly technical or major business segment product lines, special projects or strategic initiatives

 Required Qualifications:

• A minimum of a Bachelor’s Degree in a scientific, technical, or related discipline 
• A minimum of 4 years Regulatory Affairs experience in the medical industry 
• Prior experience with 510(k) submissions, EU MDR or international regulatory registrations

Preferred Qualifications:

• Prior experience with PMA submissions or Class III submissions
• Prior experience with active implantable devices, active devices, or long-term implants.
• Working knowledge of FDA, EU and international regulations for medical devices 
• General understanding of product development process, design control and quality system regulations
• Ability to simultaneously manage several projects 
• Proficiency with Microsoft Office
• Effective research and analytical skills
• Effective written and oral communication, technical writing and editing skills
• Ability to work independently with minimal supervision

Requisition ID: 627376

Minimum Salary: $89200 

Maximum Salary: $169500 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an inidual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Title: Licensed Therapist (Connecticut Licensure)

Location: United States

Job Description:

At Kindbridge Behavioral Health, we’re not just providing therapy—we’re transforming how mental health care is delivered. As a leading telehealth provider specializing in gambling, gaming, and sex/pornography process behavior disorders, in addition to mental health challenges, we are committed to expanding access to high-quality, evidence-based care.

We’re looking for Therapists licensed to practice in Connecticut (residency in CT not required) who are passionate about helping iniduals struggling with behavioral and mental health concerns. If you’re ready to make a meaningful impact while enjoying a flexible, well-supported remote practice, we’d love to hear from you.

Why Choose Kindbridge?

• Redefining Online Therapy – We streamline the administrative process so you can focus on what truly matters: client care.

• Client-First Approach – Our partnerships with gaming and gambling operators ensure a steady flow of clients who urgently need support.

• Professional Growth – We offer training, certification support (ICGC-I), and regular case consultations to help you expand your expertise.

• Work from Anywhere – Set your own hours and provide therapy from wherever you’re most comfortable, as long as you have a reliable internet connection.

What We Offer:

• Cross-State Licensing – We’ll help you obtain additional state licenses so you can serve more clients.

• Credentialing Support – We handle all insurance credentialing so you don’t have to.

• Comprehensive Admin Support – No insurance pre-authorizations, claim submissions, or collections—just focus on your clients.

• Ongoing Training – Get guidance on documentation, insurance reimbursements, and industry best practices.

• Clinical Case Consultation – Participate in regularly scheduled consults to discuss complex cases and treatment strategies.

• Cutting-Edge Tools – Access our HIPAA-compliant video platform and Learning Management System (LMS).

• Competitive 401(k) with Employer Matching – Plan for your future while making a difference today.

Who We’re Looking For:

• Therapists with active licensure in the state of Connecticut (location not a requirement)

• Bilingual (Spanish-speaking) a plus

• Willingness to complete ICGC-I certification (International Certified Gambling Counselor)

• Passion for helping iniduals with behavioral addictions and mental health challenges

• Interest in collaborating with a team that’s driving innovation in teletherapy

Join Our Mission

At Kindbridge, you’ll be part of a trailblazing team that’s making mental health care more accessible, effective, and stigma-free. If you’re looking for a flexible, rewarding opportunity to support clients struggling with behavioral addictions, apply today!

Title: Manager, Clinical Research Operations (Patient Screening)

Location: Remote - United States

Job Description:

Paradigm is rebuilding the clinical research ecosystem by enabling equitable access to trials for all patients. Our platform enhances trial efficiency and reduces the barriers to participation for healthcare providers. Incubated by ARCH Venture Partners and backed by leading healthcare and life sciences investors, Paradigm’s seamless infrastructure implemented at healthcare provider organizations, will bring potentially life-saving therapies to patients faster.

Our team hails from a broad range of disciplines and is committed to the company’s mission to create equitable access to clinical trials for any patient, anywhere. Join us, and bring your expertise, passion, creativity, and drive as we work together to realize this mission.

We are seeking a Manager of Clinical Research Coordination to lead a team of Virtual Clinical Research Coordinators  responsible for patient pre-screening across the Paradigm Health network. This role aims to improve operational excellence. It focuses on enhancing screening workflows. The goal is to quicken clinical trial enrollment using high-quality and compliant processes.

What you’ll do:

• Lead and develop a team of remote pre-screening CRCs, leading performance, accountability, and quality while effectively managing both direct and matrixed team structures

• Assess and improve site-level patient pre-screening workflows. Ensure that patient identification is efficient and reliable during the pre-screening process.

• Own operational management of pre-screening activities, including rigorous tracking, analysis, and reporting of key performance metrics to inform decision-making

• Serve as a critical bridge between leadership and frontline teams, translating strategic priorities into execution and translating insights from operations into actionable improvements in execution.

• Provide strategic oversight across the clinical research coordination function, identifying opportunities to improve processes, scale operations, and enhance site performance and patient pull through into trials.

• Drive change management initiatives, partnering with stakeholders to implement new workflows, improve adoption, and ensure alignment across teams

• Manage cross-functional relationships with clinical sites and internal partners, ensuring clear communication, effective handoffs, and alignment on enrollment goals

• Act as an escalation point for complex operational and eligibility challenges, ensuring timely resolution and minimal disruption to workflows

• Accountable for team capacity management and workload allocation across all projects and sites.

• Contribute to SOP development and continuous improvement efforts, supporting scalable and standardized processes across the full clinical research lifecycle

Who you are:

• 5+ years of experience in clinical research, healthcare operations, or related patient-facing roles, with demonstrated leadership experience (direct or matrix management)

• Deep clinical foundation, preferably with experience in clinical research operations, site workflows, and oncology

• Deep knowledge of clinical trial protocols, eligibility criteria, and protocol review processes

• Top-notch verbal and written communication skills, with the ability to influence and collaborate across erse teams

• Proven ability to manage and optimize workflows, track and analyze performance metrics, and drive process improvements in a dynamic environment

• Experience operating across the full clinical research lifecycle, with a focus on operational strategy and change management

• Ability to effectively bridge leadership and execution, translating strategic priorities into actionable plans for frontline teams

• Demonstrated success engaging clinical sites and cross-functional stakeholders to drive alignment and implement process changes

• Familiarity with EHR systems, clinical databases, and digital health platforms

• Solid knowledge of GCP, HIPAA, and applicable clinical research regulations

What You’ll Receive:

• Competitive health, dental, and vision insurance

• Mental health support for you and your family through Spring Health

• Equity package

• Unlimited paid time off (PTO)

• 16 weeks of paid parental leave

• Flexible work options – remote and hybrid arrangements

• Company-paid life insurance

• Company-paid short-term and long-term disability coverage

• One Medical membership

• 401(k) plan with company match

At Paradigm, we are committed to providing equal employment opportunities to all qualified iniduals. We encourage and welcome candidates from all backgrounds and perspectives to apply for our open positions. We are interested in all qualified iniduals and  ensure that all employment decisions are based on job-related factors such as skills, experience, and qualifications.

Sr. Design Quality Engineer

Location: Boston, Massachusetts, United States of America

Hybrid

Full-time

Job Description:

Position Description:

Sr. Design Quality Engineer for Covidien, LP (a Medtronic company):

• Perform Quality engineering activities in support of new product development.
• Work cross-functionally to review requirements and identify and assess product risks, and mitigation strategies, as well as review protocols and reports to support product validation.
• Support Systems NPD Quality team in performing engineering analysis to ensure design quality, analyzing system, and sub-system risk, technical writing, resolving high-profile quality issues, and product improvements for robust design.
• Utilize Medical device design controls, product risk files, and lean sigma methodologies, including Define, Measure, Analyze, Improve, and Control (DMAIC), Design for Reliability (DfR) and Design for Manufacturing (DfM). Utilize DOE (Design of Experiments), SPC (Statistical Process Control), Variable Gage R & R, ANOVA (analysis of Variance), t-test, regression analysis, Process Capability, Confidence & Tolerance interval analysis and process control.
• Evaluate products and process risks using d/p Failure Mode, Effects, and Criticality Analysis (FMECA), utilizing ISO 14971.
• Navigate New Product Development Life Cycle. Leverage QMS (Quality Mgmt. System) processes including CTQ (Critical to Quality) and knowledge of FDA 21 CFR part 820 ISO 13485:2003 medical device materials, related processes, and GDP (Good Documentation Practices).
• Utilize design capability, value stream and process mapping, and 5S.
• Troubleshoot production and other issues utilizing problem solving techniques, including A3 thinking, PDCA (Plan, Do, Check, Act), 5 Why’s and Ishikawa (Fishbone).
• Leverage Corrective and Preventive actions (CAPA) with use of RCA (Root Cause Analysis) to solve problems, document conditions and create solutions to avoid future problems.
• Leverage statistical software including (electronic quality mgmt. system) eQMS and Minitab. Collaborate on predictive complaint analysis and conduct post-market product performance reviews to identify and mitigate potential design and quality issues.

Relocation assistance is not available for this position.

Position works a hybrid model and will be onsite in Boston, MA–4 days per week. #LI-DNI

NOTICE: Pursuant to 20 C.F.R. § 656.10, you are hereby notified that an Application for Permanent Employment Certification will be filed for the job opportunity below. Any inidual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer at the U.S. Department of Labor as follows:

Certifying Officer

Basic Qualifications:

Masters’ Degree in Mechanical, Biomedical or Bio-Engineering or related engineering field and two (2) years of experience as a product development engineer, quality engineer or related occupation in quality engineering or product development engineering or Bachelor’s degree in Mechanical, Biomedical or Bio-Engineering or related engineering field and five (5) years of experience as a product development engineer, quality engineer or related occupation in quality engineering or product development engineering. Must possess two (2) years’ experience in each of the following: Medical device design controls, product risk files, DMAIC, DfR , DfM, and Lean Six Sigma; DOE, SPC, Variable Gage R & R, ANOVA (analysis of Variance), t-test, regression analysis, Process Capability, Confidence & Tolerance interval analysis and process control; Product and Process risk utilizing d/p FMECA and ISO 14971; New Product Development Life Cycle; QMS process, identify CTQ, FDA 21 CFR Part 820, ISO 13485 and GDP; A3 thinking, PDCA (Plan, Do, Check, Act), 5 Why’s and Ishikawa (Fishbone); CAPA and RCA; eQMS and Minitab; and Predictive Complaint Analysis.

The position is located at Covidien LP (a Medtronic company), 10 Channel Center St, Boston, MA 02210.

Salary: $136,600 to $145,200 per year

THIS POSITION QUALIFIES FOR THE MEDTRONIC EMPLOYEE REFERRAL BONUS PROGRAM AT THE LEVEL OF $1,000. Refer to the program guidelines located at InternalJobs.Medtronic.com.

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning mnimums).

Title: Community Residence Counselor- Gunderson Residence

Location: Cambridge United States

Job Description:

Site: The McLean Hospital Corporation

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

The position is for Gunderson Residence (GR) which focuses on the treatment of personality disorders (BPD, NPD, ASPD) in a multi-month residential program. Training integrates evidence based approaches in the treatment of these adults seeking treatment for severe comorbid psychopathy.

Job Summary

McLean Hospital is a comprehensive psychiatric hospital committed to providing easy access to superior quality, cost-effective mental health services in the Boston area, Massachusetts and beyond. Since 1811, McLean Hospital has been a world leader in the treatment of mental illness and chemical dependency, research into the cause of mental illness and the training of generations of mental health care providers. McLean's multidisciplinary programs treat a broad range of psychiatric illnesses across the full continuum of care. Under direction of the Program Manger, the CRC provides direct patient care and participates in therapeutic milieu within the scope of defined practice. Provides direct patient care through group and inidual counseling in accordance with current treatment plan. - Clear, concise, and timely documentation; encounter forms and shift notes. - Establishes relationships with patients that are helpful and maintains professional boundaries. - Participates in patient rounds or teams per program guidelines. - Completes assigned patient care tasks per program guidelines. - Intervenes in managing complex patient situations. - Remains awake and alert at all times while on the job. Works effectively to manage the therapeutic milieu. - Participates in leading and co-leading patient groups. - Provides and supervises community activities according to needs. This may include transporting patients to and from activities in hospital vehicles. - Provides patients with direction and supervision as needed. - Follows established program policies, procedures, and protocols. - Assumes leadership when functioning in charge counselor position by delegating duties and providing supervision when needed. - Communicates information regarding patient milieu/therapeutic environment to appropriate staff in a timely manner. Supervises patients in taking medication as prescribed. - Follows all program and hospital wide policies and procedures. - Reports and documents missed doses to appropriate staff. - Communicates observations related to medication side effects and desired effects to appropriate medical staff in a timely manner. - Supports nursing staff in assisting patient in acquiring skills to successfully self-medicate. Assists patients in their activities of daily living. - Identifies patient's strengths and deficits related to ADL's and initiates and implements interventions to meet these needs. - Assesses sleep patterns and assists patients to develop more appropriate sleep cycles notifying clinical team as necessary. - Assists patients in maintaining and keeping various appointments. Maintains a commitment to professional growth and competency. - Completes mandatory in service requirements. - Identifies areas of strengths and areas needing improvement with supervisor. - Maintains competency for treating age specific patient populations. - Uses supervision effectively to enhance professional growth and development. '- attends and Participates in rounds and case conferences When appropriate. all McLean team members are expected to consistently demonstrate Our values of integrity, compassion, respect, ersity, teamwork, excellence and innovation in their work activities and interactions. this position is represented by a collective bargaining unit.

Qualifications

High School Diploma or GED Required, Bachelors Degree Preferred No experience required. One year patient care or related experience preferred, preferably in a psychiatric setting. Skills: - Verbal and written communication skills and ability to work in collaboration with others. - Driver's license (MA, CT, NH, NY, RI, VT) preferred (varies by program), and ability to satisfactorily meet hospital driving standards. Certifications: - Medication Administration Program Certification (SELECT PROGRAMS ONLY). Applicants who are not currently MAP certified will have a specified time period from the date of hire, to successfully complete a McLean sponsored MAP certification program. Successful passing of the Medication Administration Certification is a requirement of the job. - All employees must possess basic computer skills to use a variety of electronic or online systems for communication, clinical and administrative purposes. - Required to complete electronic medical records training, and demonstrate 80% accuracy on competency test within 30 days of hire.

Additional Job Details (if applicable)

Additional Job Description

Remote Type

Onsite

Work Location

5 Spruce Avenue

Scheduled Weekly Hours

0

Employee Type

Regular

Work Shift

Rotating (United States of America)

Pay Range

$23.40 - $30.73/Hourly

Grade

MCL051

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

EEO Statement:

1600 The McLean Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all iniduals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. 

Mass General Brigham Competency Framework

At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Title: Senior Healthcare Claims Integration Analyst

Job Description:

Location: Englewood , CO / United States

Employment Type: Full-Time, Remote

Job ID: 00068641141

About Cognizant

Cognizant (NASDAQ: CTSH) engineers modern businesses. We help our clients modernize technology, reimagine processes, and transform experiences so they can stay ahead in a fast‑changing world. Together, we're improving everyday life.

Job Summary

We are seeking a Claims System Integration Analyst to support system integration (SI) activities for a Proof of Concept (POC) focused on healthcare claims processing. In this role, you will partner with business, EDI, and technical teams to define requirements, validate data flows, and ensure the accuracy and integrity of historical claims data across systems.

This position requires strong healthcare payer knowledge, hands-on claims expertise, and the ability to collaborate across teams to analyze, validate, and resolve data-related issues.

Responsibilities

• Gather, analyze, and document business and technical requirements related to healthcare claims (837) and remittance (835) processing
• Support data mapping activities for claims and historical claims datasets across integrated systems
• Assist with data validation, reconciliation, and parity checking to ensure accuracy and completeness of claims data
• Collaborate closely with EDI and System Integration teams to analyze, troubleshoot, and resolve data flow and quality issues
• Support defect analysis, root cause identification, and remediation related to claims and data validation
• Contribute to POC deliverables by ensuring alignment between requirements, data, and system behavior

Required Qualifications

• Healthcare payer domain experience with a strong focus on claims processing
• Solid understanding of the end‑to‑end claims lifecycle and adjudication processes
• Experience working with HIPAA EDI transactions, specifically 837 and 835
• Strong SQL and data analysis skills for validation, reconciliation, and issue investigation
• Proven experience supporting data validation, reconciliation, and defect analysis activities
• Ability to work collaboratively with cross-functional technical and business teams

Preferred Qualifications

• Experience working with Facets or similar core claims platforms
• Prior experience supporting system integration initiatives or POCs
• Familiarity with data mapping tools, parity testing, or large-scale data migrations

Why Cognizant

• Opportunity to work on impactful healthcare transformation initiatives
• Collaborative, erse, and inclusive work environment
• Exposure to modern integration and data-driven healthcare platforms
• Competitive compensation and comprehensive benefits

Equal Opportunity Statement

Cognizant is an equal opportunity employer and is committed to creating a erse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, disability, or protected veteran status.

The annual salary for this position will be in the range of $113K-$132K depending on experience and other qualifications of the successful candidate.

This position is also eligible for Cognizant's discretionary annual incentive program, based on performance and subject to the terms of Cognizant's applicable plans.

Benefits: Cognizant offers the following benefits for this position, subject to applicable eligibility requirements:

• Medical/Dental/Vision/Life Insurance
• Paid holidays plus Paid Time Off
• 401(k) plan and contributions
• Long-term/Short-term Disability
• Paid Parental Leave
• Employee Stock Purchase Plan

Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.

POSITION: Regional Manager (RN license required)

Job Description:

Wexford Health Sources, Inc. is one of the nation’s largest correctional health care providers.  Over the past 30 years, our team of dedicated clinical professionals has helped millions of justice-involved patients receive life-changing medical and mental health services.

The majority of our patients come from marginalized or impoverished backgrounds.  In many cases, our doctors, nurses, and behavioral health professionals represent the patient’s first experience with quality, compassionate health care.

BENEFITS

• Performance check-ins with annual merit increase
• Generous paid-time off program that combines vacation and sick leave
• Paid holidays
• Comprehensive health insurance through BlueCross BlueShield
• Dental and Vision insurance
• 401(k) retirement saving plan
• Company-paid short-term disability
• Healthcare and dependent care spending account
• Continuing education options

POSITION SUMMARY

• Provides day-to-day leadership of the operation of facility health care units. Provides facility-level management staff with guidance, strategies for facility growth, and operational assistance.

• Conducts periodic staff meetings, and attends facility meetings and training as required.

• Oversees resolution of health care unit personnel issues or complaints, and directly intervenes in problem areas as needed to ensure prompt resolution, involving facility administration, contractors, if applicable, and Wexford Human Resources, as appropriate.

• Enforces compliance with all human resources policies, procedures and programs including workforce planning, recruiting, training and development, compensation and benefits, performance evaluation, and on-boarding.  Provides direction and clarity to sites to facilitate effective team dynamics.

• Works with regional personnel to develop objective performance measurements to ensure consistent, high-quality evaluation and goal setting for all sites.

• Assists in the recruitment of qualified site-level health services staff.  Participates in interviewing and hiring, and approving final selection of new employees.

• Performs performance management functions and supervises performance by conducting coaching “check-ins” and recommends/approves site-level employee developmental interventions when necessary.

• Ensures the availability of in-service education for health service staff, to comply with WVDCR, Wexford Health and accrediting agency standards. 

• Instills a sense of accountability among the sites through fair and consistent oversight of inidual and organization performance standards.

• Interacts with WVDCR and facility authorities to facilitate timely and efficient delivery of health care services.

• Monitors labor cost and overtime expenditure, ensuring sites are working within budget.

• Implements procedures to comply with administrative and institutional directives of the facilities and the WVDCR.

• Makes sound decisions regarding management and administration of health care services throughout state.

• Reviews daily, weekly, and/or monthly statistical reports.

• Reviews facility Position Control Reports to ensure adherence to staffing contractual obligations.

• Monthly review of Financial Reports for area of responsibility. Explanations of variances, trends, unusual expenses will be required.

• Reviews office, medical, mental health, etc. supply orders being submitted.

• On-going, routine communication with WVDCR facility administration (Warden, etc.) to ensure site-level client satisfaction.

• Facilitates routine meetings and perform functions required by administrative directives, including Quality Assurance, Chronic Clinics, Pharmacy and Therapeutics, and Health Care.

• Helps respond to Corporate Risk Management Department inquiries regarding complaints or grievances by patients, family members, lawyers or other advocates.  Assists with legal proceedings as needed.

• Participates in preparatory, WVDCR and credentialing organization audits of health services.

• Helps develop, implement, and monitor corrective action plans designed to resolve audit findings.

• Works jointly with regional training staff and Corporate Training and Program Development Specialist to ensure that appropriate training and New Employee Orientation is available to comply with contract requirements state-wide.

• Monitors the systems, processes and tools to better support the facilitation, collection, and sharing of knowledge generated by the regional office.

• Supports the development of inter-team communication and cohesiveness, sustaining culture and supporting staff during organizational change and growth.

• Participates in local, regional, and national representative meetings related to the trends and developments in Wexford Health and correctional health care.

JOB REQUIREMENTS

LICENSURE:  Valid, unrestricted West Virginia Registered Nurse license preferred

Title : Senior Facets Integration Analyst

Job Description:

Location: Remote

Employment Type: Full-Time

Job ID: 00068642041

Job Title: Senior Facets Integration Analyst

About the role

As a Senior Facets Integration Analyst, you will make an impact by supporting the configuration and validation of the Facets core claims platform for a healthcare Proof of Concept (POC). This role focuses on benefits setup, configuration accuracy, and alignment with real-world claims processing scenarios. You will be a valued member of the System Integration team and work closely with claims, EDI, and testing stakeholders to ensure accurate claims adjudication outcomes.

In this role, you will:

• Configure Facets components to support healthcare claims processing scenarios, including benefits, rules, pricing, and related configuration elements
• Validate Facets configuration against expected claims adjudication outcomes to ensure accuracy and parity
• Collaborate with System Integration and EDI teams to confirm alignment between Facets configuration, incoming claims transactions (837), and expected remittance outputs (835)
• Assist with troubleshooting and resolving configuration-related issues that impact claims adjudication and parity validation
• Support testing and validation cycles through analysis of claim scenarios, outcomes, and configuration behavior
• Document configuration decisions, dependencies, and assumptions to support POC delivery and knowledge transfer

Work model

We strive to provide flexibility wherever possible. Based on this role's business requirements, this is a remote position. Regardless of location, we are committed to supporting a healthy work‑life balance through our wellbeing programs.

The working arrangements for this role are accurate as of the date of posting and may evolve based on project or client needs. We will always be transparent about role expectations.

What you need to have to be considered

• Hands-on experience with Facets configuration, including benefits, pricing, or claims setup
• Strong understanding of healthcare claims adjudication processes
• Healthcare payer experience is required
• Ability to analyze claims scenarios and assess expected versus actual outcomes
• Experience supporting testing, validation, and defect resolution cycles

These will help you stand out

• Experience supporting system integration initiatives or Proofs of Concept (POCs)
• Familiarity with HIPAA EDI transactions, including 837 and 835
• Strong analytical and problem-solving skills with attention to configuration detail
• Experience working with cross-functional technical and business teams

Salary and Other Compensation:

Cognizant will only consider applicants for this position who are legally authorized to work in the United States without company sponsorship.

• Please note, this role is not able to offer visa transfer or sponsorship now or in the future*

The annual salary for this position will be in the range of $113K-$132K depending on experience and other qualifications of the successful candidate.

This position is also eligible for Cognizant's discretionary annual incentive program, based on performance and subject to the terms of Cognizant's applicable plans.

Benefits: Cognizant offers the following benefits for this position, subject to applicable eligibility requirements:

• Medical/Dental/Vision/Life Insurance
• Paid holidays plus Paid Time Off
• 401(k) plan and contributions
• Long-term/Short-term Disability
• Paid Parental Leave
• Employee Stock Purchase Plan

Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.

Our strength is built on our ability to work together. Our erse backgrounds offer different perspectives and new ways of thinking. It encourages lively discussions, creativity, productivity, and helps us build better solutions for our clients. We want someone who thrives in this setting and is inspired to craft meaningful solutions through true collaboration.

If you are content with ambiguity, excited by change, and excel through autonomy, we'd love to hear from you!

Apply Now!

#LI-IK1

Title: Senior Manager, Data Governance & Data Integrity, Computer System Validation Program

Job Description:

Location:  remote, United States

Category: Quality

Senior Manager, Data Governance & Data Integrity, Computer System Validation Program for Quality

Who We Are

BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.

Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.

Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a erse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.

About Technical Operations

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

SUMMARY DESCRIPTION

The Senior Manager, Data Governance & Data Integrity (DG/DI) and CSV/CSA Program will own and advance two critical, interdependent quality programs that underpin enterprise regulatory compliance and operational excellence within the global Quality organization and Technical Operations. The DG/DI program has established a strong foundation and now requires focused maturation — building program depth through defined KPIs, metrics, and maturity assessments; continuously strengthening alignment with evolving global regulatory requirements; and integrating emerging technology considerations such as AI/ML data integrity requirements into the QMS. The CSV/CSA program is an established enterprise function but is fragmented across the business, creating cost inefficiencies and inconsistency in execution; this role will drive harmonization of the CSV/CSA framework to achieve a unified, risk-based approach across all sites and functions.

The ideal candidate possesses deep expertise in data integrity, data governance, and GxP computerized system validation, with a demonstrated ability to mature and harmonize programs across a complex, multi-site enterprise. They bring strong command of evolving global regulatory expectations — including AI/ML validation frameworks, EU GMP Annex 11, and Computer Software Assurance — and can translate those requirements into practical program enhancements that keep the organization ahead of the compliance curve. The ideal candidate will assess program maturity, define meaningful KPIs and metrics, and identify gaps and priorities that drive continuous improvement across both disciplines. In this role, you will serve as the enterprise subject matter expert and the central force for elevating DG/DI program maturity and unifying a fragmented CSV/CSA landscape — reducing cost and inefficiency while building long-term organizational capability and regulatory resilience.

RESPONSIBILITIES

DG/DI Program – Quality Assurance Oversight & Program Enhancemen

• Serve as the enterprise subject matter expert for data integrity, data lifecycle management, ALCOA+ principles, and GxP data governance frameworks (FDA, EMA, MHRA, WHO, PIC/S); define program strategy, KPIs, and maturity assessments to drive measurable and sustained DG/DI program enhancement.
• Lead the integration of Data Integrity by Design (DI by Design) principles into QMS processes, procedures, and system design; establish program maturity benchmarks and track enterprise-wide progress against defined targets.
• Support site and function DI gap assessments and remediation strategy; identify compliance risks, drive visibility and resolution with DI Leads and site management, and provide expert technical guidance and direction.
• Design the enterprise DG/DI training model and co-develop role-based curricula in partnership with global and site training coordinators and DI Leads, building sustained data integrity capability across the organization.
• Lead the DG/DI Governance Program and Quality Plan; ensure DI Leads maintain progress against commitments, escalate issues to executive management, and present program status, risk landscape, and key metrics at Quality Management and Quality System review forums.
• Serve as the primary DG/DI subject matter expert for internal and external audits and regulatory inspections; prepare supporting documentation, respond to findings, and ensure remediation is tracked to closure.
• Own the DG/DI QMS SOPs and supporting procedures; ensure harmonization and alignment across the QMS hierarchy and consistent application of DI requirements enterprise wide.
• Monitor and translate emerging regulatory requirements (EU GMP Annex 11 revised, Annex 22, Chapter 4, AI/ML DI frameworks, FAIR data principles) into actionable QMS and program updates; cultivate strong partnerships with IT, CSV leads, DI Leads, BPOs, and system owners to secure alignment and ensure sustained adoption.

Enterprise Computerized System CSV/CSA – Quality Assurance Project Support

• Provide QA oversight and strategic direction for enterprise computerized system CSV/CSA programs; define validation strategy, GxP applicability determinations, and risk-based approaches across the full system lifecycle — partnering with IT, system owners, and project teams who execute.
• Drive harmonization of a fragmented enterprise CSV/CSA landscape; establish a unified, risk-based framework aligned with FDA CSA guidance and GAMP 5 that eliminates redundancy, reduces cost, and improves consistency across sites and functions.
• Review and approve CSV/CSA deliverables including validation strategy, GxP applicability assessments, URS, risk assessments, traceability matrices, test protocols, and validation summary reports; translate regulatory requirements into practical QMS and project-level requirements.
• Provide QA guidance on changes to validated computerized systems; assess scope and impact, determine appropriate validation or re-validation requirements, and maintain oversight of the enterprise validated systems inventory.
• Develop and maintain the CSV/CSA program KPI framework, providing DI Leads, system owners, and management with meaningful visibility into program performance and areas requiring attention; champion integration of AI/ML and cloud/SaaS considerations into the CSV/CSA quality framework.
• Serve as the primary CSV/CSA QA resource for internal and external audits and regulatory inspections; ensure program documentation supports inspection readiness and partner with project teams to resolve findings.

QUALIFICATIONS

Required

• Bachelor’s degree in Life Sciences, Engineering, Computer Science, or a related field; advanced degree preferred.
• 10+ years of progressive experience in a GxP-regulated pharmaceutical, biotechnology, or life sciences environment, with a clear track record of increasing program ownership and scope.
• Proven track record of leading and establishing enterprise DG/DI governance programs and/or QMS data integrity requirements from the ground up or through significant maturation; candidates with only site-level or execution-focused DI experience will not be considered.
• Extensive experience in GxP computerized system lifecycle management (CS LCM) spanning manufacturing systems (MES, SCADA, DCS, automation), Quality and Clinical Quality systems (QMS, LIMS), and enterprise platforms.
• Experience with systems modernization programs, cloud and SaaS validation strategies, and application of CSA principles to emerging technology platforms.
• Deep working knowledge of 21 CFR Part 11, EU GMP Annex 11, GAMP 5, ALCOA+ principles, ISPE Good Practice Guides, ICH Q9/Q10, and FDA/MHRA/EMA/WHO data integrity guidance; working knowledge of emerging requirements including Annex 11 (revised draft), Annex 22, Chapter 4, and AI/ML validation frameworks.
• Demonstrated experience leading cross-functional DG/DI or CSV/CSA governance bodies, quality forums, or enterprise working groups; able to operate effectively at the program strategy level and influence senior stakeholders without direct authority.
• Proven ability to lead enterprise or multi-site DG/DI programs at the governance and strategy level, including program design, QMS SOP ownership, maturity assessments, KPI frameworks, and regulatory inspection support as a subject matter expert.
• Strong understanding of electronic QMS platforms (e.g., Veeva Vault) and how DI principles are embedded throughout quality systems.
• Excellent communication skills with demonstrated ability to influence cross-functionally without direct reporting authority in a matrixed environment.
• Experience participating in health authority inspections as a CSV/CSA or DI subject matter expert.

Preferred

• Working knowledge of AI/ML model validation, data integrity requirements for AI-enabled GxP systems, and application of emerging FDA/IMDRF AI/ML frameworks to Quality and manufacturing contexts.
• Background in data lifecycle management and FAIR data principles as applied to GxP environments, experience with enterprise data governance platforms and electronic records management strategies.
• Proficiency with data visualization and QMS analytics tools (e.g., Power BI, Veeva reporting).
• ISPE GAMP, ASQ or equivalent professional certification in Data Governance or CSV/CSA disciplines.
• Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Workstyle:

• This is a virtual position unless you live within 100 miles of Novato, Ca (zip code 94903).  If so, then the role reverts to hybrid requiring being onsite twice a week.

Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Title: Licensed Mental Health Counselor/Marriage & Family Therapist (LMHC & LMFT) - Remote

Location: Florida (Remote)

Work Type: Remote, Full Time

Compensation

• $68K – $74K • Offers Bonus • Total earning opportunity reaching $100k annually for top earners

Department: Clinical-Therapist

Job Description:

Why We're Here:

Job description

We are looking for full-time Licensed Therapists to join our team and provide outpatient services through our telehealth program!

Benefits: Our team works 100% remotely from their own homes!

• W2, Full-time

• Compensation package includes base salary plus bonus!

• Monday - Friday schedule; No weekends! Shift options include 9am-6pm, 10am-7pm, 11am-8pm Eastern

• Comprehensive benefits package including PTO, medical, dental, vision benefits along with liability insurance covered and annual stipend for growth & education opportunities

• Additional compensation offered to bilingual candidates (Spanish)!

• We not only partner with commercial health plans, but are also a licensed Medicaid and Medicare provider and see patients across the lifespan

Requirements:

• Master's level degree and licensure

• Candidates must have unrestricted authorization to work in the United States that does not require employer sponsorship now or in the future. At this time, we are unable to support employment authorization tied to temporary or employer-dependent visa statuses.

• Work from home space must have privacy for patient safety and HIPAA purposes

• Fluency in English, Spanish preferred; proficiency in other languages a plus

Skills:

• Knowledge of mental health and/or substance abuse diagnosis

• Treatment planning

• Comfortable with utilizing technology at all points of the day, including telehealth software, video communication, and internal communication tools

• Experience working in partnership with clients to achieve goals

• Ability to utilize comprehensive assessments

Title: Clinical Care RN

Location: Atlanta, GA

Job Description:

Location: Hybrid within 30 miles of Atlanta, GA

Job Type: Full Time, M-F 8:30am-5pm

Job Reports To: Director of Clinical Operations

About Jaan Health/Phamily 

Jaan Health is a leading AI-based care management company serving healthcare providers. For nearly a decade, the company has leveraged its easy-to-use, proprietary technology to enable health systems, medical groups, and ACOs to deliver high-quality, high-ROI proactive care to hundreds of thousands of previously underserved patients.

Phamily, the company's core technology platform, has transformed chronic disease management with clinically tested AI and easy-to-use technology that enables physicians and care teams to offer high-touch, inidualized patient care that has been proven to reduce investment in extra labor and the overall cost of care.  Phamily helps ensure healthcare providers are compensated fairly for providing high-quality care between office visits, while improving the lives of patients with chronic diseases. Learn more at phamily.com.

Job Role/Description

We are seeking a compassionate, organized, and tech-savvy Clinical Care Lead RN to support patients in our text-based Advanced Primary Care Management (APCM) program. This role focuses on delivering proactive, high-quality care through digital communication tools, driving better health outcomes for our patient populations. Ideal for healthcare professionals who thrive in a virtual care setting, value patient engagement, are passionate patient advocates and are skilled in critical thinking and care coordination.

Key Responsibilities

• Monitor and respond to patient messages and check-ins in a timely, compassionate, and professional manner
• Identify, assess, and triage clinical concerns, SDOH needs, and care coordination barriers
• Develop and update personalized care plans for patients; help educate and motivate patients to adhere to the care plan
• Oversee the clinical quality of the team, by analyzing data or trends to manage direct reports, and help train, orient, and onboard new and tenured staff, and improve overall outcomes
• Develop, implement, and revise care coordination workflows or protocols to support the evolution of the care model to improve efficiency and scalability
• Lead quality improvement initiatives, complete case review and chart audits, and host team meetings
• Identify and troubleshoot issues that arise during new program iterations, escalating to leadership when there are critical impacts or opportunities for system-wide improvements
• Collaborate with CMAs, LPNs/RNs, NPs, and Social Workers to ensure timely escalation and follow-through

Requirements

• Registered Nurse with active, unrestricted compact license required with 4+ years of experience in a care management or clinical care coordination role (primary care, chronic care management, home health, etc.)
• Previous experience managing a team
• Strong critical thinking and problem-solving skills in a fast-paced environment
• Ability to independently manage a digital patient panel and prioritize escalations effectively
• Excellent written communication and documentation skills
• Comfort using EMRs, care coordination platforms, digital messaging tools and fast learner of new technologies
• Must have access to reliable internet and a secure/private environment
• This role may require travel of up to 10%, including potential overnight travel

Preferred Requirements 

• 4+ years of experience, 2-year RN Associate Degree OR 2+ years experience + BSN
• Bilingual (Spanish) is a bonus but not required
• Knowledge of Medicare CCM/APCM programs a plus

Compensation & Benefits 

• Competitive compensation commensurate with experience
• Potential to earn equity based on performance
• Medical, dental, and vision coverage for employees and dependents at a nominal cost
• Paid maternity leave
• FSA and Dependent Care account options
• 401(k) Eligibility after 6 months of full-time employment 
• Collaborative, mission-driven work environment

If you take pride in delivering results, embrace challenges, and proactively seek improvement, then this is the place for you. You’ll join a smart, humble, and collaborative team dedicated to improving healthcare. 

Equal Employment Opportunity 

Phamily is an equal opportunity employer. We celebrate ersity and are committed to creating an inclusive environment for all employees. Employment decisions are made without regard to race, color, religion, sex, national origin, age, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other legally protected status.

Title: Associate Consultant, Life Sciences Consulting (Market Access)

Job Description:

Company: Dedham Group

Description

About The Dedham Group  

We set out to develop a health care innovation organization that could separate the background “noise” from what warrants investment in our highly complex, rapidly evolving marketplace lacking transparency to enable our pharmaceutical and biotech clients to make better decisions and flourish.   

Today, ten years later, we are the preeminent U.S. market access oncology and specialty strategy partner, grounded in the structure and logic of the strategy consulting discipline, bolstered by our robust data set continuously enriched via our unequaled specialty access panel of the most highly influential access and value influencers in the U.S.   

With a unique staffing model of highly structured and collaborative creative thinkers akin to an oncology and specialty think tank, we have increasingly come to be viewed as an influencer in our industry. At the interface of clinical, economic, and operational evolving needs, the Dedham Group has become the go-to resource for addressing the challenges faced by the world’s leading life sciences organizations.   

Now, The Dedham Group is proud to be a part of Norstella, an organization that consists of market-leading pharmaceutical solutions providers united under one goal: to improve patient access to life-saving therapies. Within this organization, The Dedham Group plays a key role helping commercial teams navigate the oncology space to get much-needed drugs to market—and helping clients connect the dots from pipeline to patient.   

About the role:    

As an Associate Consultant, you will support Consultants and Senior Consultants in day-to-day management of projects, helping guide overall strategic direction and delegating tasks to team members. To succeed in this role, you will:     

• Support Consultants, Senior Consultants, and Engagement Managers in day-to-day management of project activities, assisting to guide overall strategic direction and delegating tasks to team members. 
• Assist in training and development of interns and new hires (Analysts and Senior Analysts), oversee intern and analyst workstream progress to ensure project timelines are met, and provide feedback to junior staff. 
• Scope deck structure, slide structures and key analyses for inclusion to ensure linear story flow and clear communication of key points impactful to client. 
• Oversee primary and secondary research relevant to project output to ensure key insights are gathered. 
• Participate in client meetings to position oneself as a subject matter expert by citing specific insights to solidity credibility with clients; support email-based communication (e.g., meeting scheduling, question fielding) as appropriate; fulfill ongoing client requests for staffed projects.
• Communicate clearly with senior project managers on project responsibilities, progress, alignment to timeline, bandwidth of team to offer additional support, and proactive outreach on any questions or support needs to streamline project execution.
• Develop detailed project timelines for team to follow to ensure time execution; proactively structure deliverables to ensure organized, MECE and linear logic through project execution. 
• And other duties as assigned.

Qualifications:

• Bachelor’s or advanced degree with a life science focus    
• 3+ years of life sciences Market Access consulting experience
• Superior skills in using MS Office (particularly PowerPoint and Excel)  
• Excellent oral and written communication skills   
• Strong collaboration skills; must be a team player   
• Strong attention to detail  
• Strong knowledge of provider and payer dynamics within healthcare, specifically within oncology, cellular therapy / CAR-T, immunology, neurology / CNS, and or other rare diseases / specialty therapeutics

The guiding principles for success at Norstella:    

01:  Bold, Passionate, Mission-First     

We have a lofty mission to Smooth Access to Life Saving Therapies and we will get there by being bold and passionate about the mission and our clients.  Our clients and the mission in what we are trying to accomplish must be in the forefront of our minds in everything we do.      

02:  Integrity, Truth, Reality    

We make promises that we can keep, and goals that push us to new heights.  Our integrity offers us the opportunity to learn and improve by being honest about what works and what doesn’t.  By being true to the data and producing realistic metrics, we are able to create plans and resources to achieve our goals.      

03:  Kindness, Empathy, Grace    

We will empathize with everyone's situation, provide positive and constructive feedback with kindness, and accept opportunities for improvement with grace and gratitude.  We use this principle across the organization to collaborate and build lines of open communication.      

04:  Resilience, Mettle, Perseverance    

We will persevere – even in difficult and challenging situations.  Our ability to recover from missteps and failures in a positive way will help us to be successful in our mission.    

05:  Humility, Gratitude, Learning    

We will be true learners by showing humility and gratitude in our work.  We recognize that the smartest person in the room is the one who is always listening, learning, and willing to shift their thinking.      

Benefits:

• Medical and prescription drug benefits
• Health savings accounts or flexible spending accounts
• Dental plans and vision benefits
• Basic life and AD&D Benefits
• 401k retirement plan
• Short- and Long-Term Disability
• Education benefits
• Paid parental leave
• Open Vacation Policy

Please note – all candidates must be authorized to work in the United States. We do not provide visa sponsorship or transfers and are not currently accepting candidates who are on an OPT visa.  

The expected base salary for this position ranges from $130,000 to $150,000. It is not typical for offers to be made at or near the top of the range. Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, licensure or certifications obtained. Market and organizational factors are also considered. In addition to base salary and a competitive benefits package, successful candidates are eligible to receive a discretionary bonus.   

All legitimate roles with Norstella will be posted on Norstella’s job board which is located at norstella.com/careers. If a role is not posted on this job board, a candidate should assume the role is not a legitimate role with Norstella. Norstella is not responsible for an application that may be submitted by or through a third-party and candidates should proceed with extreme caution if a third-party approaches them about an open role with Norstella. Norstella will never ask for anything of value or any type of payment during or as part of any recruitment, interview, or pre-hire onboarding process. If you are aware of or have reason to believe a job posting purportedly for a role with Norstella is fraudulent or otherwise not authorized by Norstella, please contact the Company using the following email address: [email protected]. 

The Dedham Group is an equal opportunity employer. All Job applicants will receive equal treatment regardless of race, creed, color, religion, alienage or national origin, ancestry, citizenship status, age, physical or mental disability or handicap, medical condition, sex (including pregnancy and pregnancy-related conditions), marital or domestic partner status, military or veteran status, gender, gender identity or expression, sexual orientation, genetic information, reproductive health decision making, or any other protected characteristic as established by federal, state, or local law. 

Sometimes the best opportunities are hidden by self-doubt. We disqualify ourselves before we have the opportunity to be considered. Regardless of where you came from, how you identify, or the path that led you here- you are welcome. If you read this job description and feel passion and excitement, we’re just as excited about you.

Title: Staff Engineer - FPGA Engineering

Location: London, Cambridge UK

Type: Full Time

Workplace: hybrid

Category: Meridial

Job Description:

About Meridial

Meridial is a Focused Research Organisation (FRO) with a mission to bring connectomics into the living brain. We are building a platform for longitudinal, synapse-resolution mapping of functional neural circuitry in preclinical models. Our aim is to deploy this platform for translational projects and improve drug development outcomes for disorders of the Central Nervous System.

Meridial is a new not-for-profit FRO in the Convergent Research Ecosystem and powered by the Advanced Research and Invention Agency (ARIA).

About the role

Meridial is seeking an entrepreneurial FPGA Engineer to join as a core technical contributor on our multi-photon microscopy platform. This is a hands-on role spanning FPGA architecture development and iterative system improvement. This role reports to the Director of Engineering, working in close partnership with our neuroscience and engineering teams. You will take ownership of the FPGA systems at the heart of our microscopes - maintaining and supporting current platforms, extending the existing codebase, and helping shape and build future architectures as our platform grows in capability and ambition.

The position calls for substantial practical experience with FPGA development and judgment to deeply engage with both legacy and next-generation architectures, including porting code across devices, evaluating hardware options, and making sound design decisions across interfaces, logic, and memory subsystems. It will also involve working closely with users and collaborators to understand technical needs, debug complex issues, and implement new functionality effectively. The ideal candidate will demonstrate strong FPGA engineering fundamentals and a startup-friendly mindset that keeps development moving forward in a fast-paced build-and-iterate environment.

Key Responsibilities

• Lead the development of next-generation FPGA systems at the heart of our microscopy platform — taking ownership of the existing codebase and its future evolution
• Evaluate hardware options and design trade-offs across PC interfacing, device communication, logic structure, and memory subsystems
• Port existing FPGA designs to new devices and platforms while preserving performance, reliability, and maintainability
• Maintain, debug, and improve FPGA implementations, diagnosing issues across firmware, hardware interfaces, and system-level behaviour
• Collaborate closely with neuroscientists and engineers to understand system requirements and translate them into firmware solutions with clear technical specifications 
• Contributing to documentation and development practices
• Help define and raise our technical ambitions — identifying problems we have not yet seen and proposing creative solutions

Required Qualifications

• Degree in Electronic Engineering, Computer Science, Physics, or a closely related field
• Significant hands-on experience developing FPGA systems for complex instruments, embedded platforms, or high-performance hardware applications
• Very strong experience with VHDL or a similar hardware description language
• Experience working with Xilinx FPGA devices, including development, debugging, and porting between parts or families
• Experience with multiple FPGA vendors or device families beyond Xilinx, with the ability to adapt designs across platforms
• Strong understanding of FPGA architecture and digital system design, including interfaces, timing closure, memory subsystems, and system-level trade-offs
• Demonstrated ability to take ownership of an existing codebase, improve it, and guide its long-term architectural direction
• Ability to move fluidly between implementation and higher-level architecture — making good engineering decisions while keeping development practical and forward-looking
• Strong debugging skills, with the ability to isolate and resolve issues across FPGA logic, surrounding electronics, and software/hardware boundaries
• Strong communication skills and a collaborative mindset — you can explain a complex technical trade-off to non-specialists and turn user feedback into clear engineering requirements

Preferred Qualifications

• Industry or startup experience in instrumentation, embedded systems, scientific hardware, or related high-performance engineering environments — you know how to apply the theory and what it means to build something that has to work reliably
• Experience with the hardware side of FPGA systems, including board-level bring-up, signal interfacing, and integration with surrounding electronics
• Experience developing custom FPGA boards or FPGA module carrier boards (specification, design, debugging). 
• Experience with National Instruments FPGA systems and their associated development workflows
• Familiarity with high-speed interfaces, data acquisition systems or real-time control in demanding hardware environments
• Experience working on systems where FPGA, software, and hardware co-design are tightly linked
• Programming ability beyond VHDL — enough to interface with test infrastructure, automation, or diagnostic tooling where needed (Rust highly desirable)

Physical Demands

• Fine motor skills for operating computers and lab/instrumentation tools
• Ability to move light-to-moderate items (typical lab supplies/computers); may include occasional lifting/carrying with appropriate equipment (e.g., carts/dollies, kit)

Position Type / Schedule

• Full-time at 40 hours/week preferred but will consider freelance contracting for the right fit
• Lab location based in London or Cambridge — ability to travel to both preferred
• Work arrangement: Hybrid with expected regular onsite presence due to laboratory responsibilities

Additional Information

• For exceptional candidates, we will consider sponsoring visas and supporting relocation
• Compensation: competitive salary commensurate with experience
• Generous Benefits will be communicated in interviews

£80,000 - £100,000 a year

We are an Equal Employment Opportunity employer and do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable law or company policy. We strive for a erse, healthy and safe workplace and strictly prohibit harassment of any kind.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Title: Engineer / Sr. Engineer - Optics and Photonics

Locations:  London or Cambridge

Type: Full Time

Workplace: hybrid

Category: Meridial

Job Description:

About Meridial

Meridial is a Focused Research Organisation (FRO) with a mission to bring connectomics into the living brain. We are building a platform for longitudinal, synapse-resolution mapping of functional neural circuitry in preclinical models. Our aim is to deploy this platform for translational projects and improve drug development outcomes for disorders of the Central Nervous System.

Meridial is a new not-for-profit FRO in the Convergent Research Ecosystem and powered by the Advanced Research and Invention Agency (ARIA).

About the role

Meridial is seeking an entrepreneurial Optics & Photonics Engineer to join as a core technical contributor on our multi-photon microscopy platform. This is a hands-on role spanning optical system design, prototyping, iterative development and maintenance in close partnership with our neuroscience and engineering teams. This role reports to the Director of Engineering. You will own the optical stack end-to-end — from ultrafast laser source to sample and detector — and play an active part in identifying and solving technical challenges as our platform grows in capability and ambition.

The position calls for substantial practical experience with multi-photon microscopy and the ability to engage deeply with custom optical design, including working directly with specialty manufacturers to specify and refine components beyond off-the-shelf solutions. It will also involve interfacing with expert contractors who have deep familiarity with specific aspects of our platform, so a genuine eagerness to learn quickly and apply that knowledge effectively is essential. More broadly, the ideal candidate will bring strong optical engineering fundamentals and a startup-friendly mindset that keeps development moving forward in a fast-paced build-and-iterate environment.

Key Responsibilities

• Lead the optical design, prototyping, alignment, and characterisation of our two-photon microscopy platform and its extensions — taking ownership of the full system from ultrafast laser source to the sample and detector

• Develop and iterate on Zemax (or equivalent) optical models; critically evaluate vendor-supplied designs and push them beyond conservative defaults to meet our performance targets

• Drive the commissioning of custom optical components, including custom objective lenses — working directly with specialist manufacturers, understanding their design constraints, and independently modifying or extending their models

• Stay current with emerging optical fabrication and design technologies and proactively identify opportunities to incorporate them into our platform

• Collaborate closely with neuroscientists and engineers to deeply understand imaging requirements and translate them into optical system specifications

• Contribute to mechanical design of optical assemblies and opto-mechanical mounts

• Maintain, troubleshoot, and continuously improve existing microscope systems; develop alignment procedures and documentation that scale with the team

• Help define and raise our technical ambitions — identifying problems we haven't yet seen and proposing creative solutions

Required Qualifications

• Degree in Optics, Photonics, Physics, Biomedical Engineering, or a closely related field

• Significant hands-on experience designing, building, and characterising complex optical systems — ideally custom research microscopes including multi-photon systems or other high-performance imaging instruments

• Proficiency in optical design software (Zemax OpticStudio or equivalent)

• Strong working knowledge of imaging optics fundamentals: aberration theory, Fourier optics, coherence, nonlinear optical processes, and ultrafast laser physics as they apply to multiphoton imaging

• Demonstrated ability to move fluidly between simulation/modeling and physical hardware 

• Programming ability — enough to write acquisition scripts, automate alignment routines, process and visualize optical characterization data, and interface with hardware (Python preferred; MATLAB acceptable)

• Experience engaging with optical vendors and custom component manufacturers; ability to critically assess and modify third-party optical designs

• Strong communication skills and a collaborative mindset — you can explain a complex optical trade-off to a biologist and take feedback from a neuroscientist and turn it into a design requirement

Preferred Qualifications

• Ph.D. in Optics, Photonics, Physics, Biomedical Engineering, or a closely related field

• Industry or startup experience in the field  (optical engineering, photonics, instrumentation etc) or postdoctoral research experience, particularly in a lab developing novel microscopy instrumentation — you know how to apply the theory and what it means to build something that has to work reliably

• Experience with custom objective lens design and/or commissioning, including immersion objectives, high-NA systems, or specialty wavelength ranges

• Experience with Acousto-optics and Electro-optics

• Experience with photodetectors (PMTs, Avalanche Photodiodes, photon counting)

• Experience with laser systems, ultrafast pulse characterization, beam delivery, and photonics integration in experimental setups

• Familiarity with CAD tools (SolidWorks, Fusion 360, or similar) for opto-mechanical design; experience with rapid prototyping workflows (3D printing, machine shop coordination)

• Experience or strong familiarity with three-photon microscopy

• Experience with advanced two-photon system extensions: adaptive optics, spatial light modulators (SLMs), temporal focusing, or related wavefront/pulse shaping techniques

• Familiarity with fiber optics and gradient-index (GRIN) lens systems for minimally invasive or endoscopic imaging applications

Physical Demands

• Fine motor skills for operating computers and office/lab equipment

• Ability to move light-to-moderately heavy items (typical lab supplies/equipment); may include occasional lifting/carrying with appropriate equipment (e.g., carts/dollies

Position Type / Schedule

• Full-time, 40 hours/week

• Lab location based in London or Cambridge - ability to travel to both preferred

• Work arrangement: Hybrid with expected regular onsite presence due to laboratory responsibilities

Additional Information

• Application materials: CV/resume + cover letter + 2 references

• For exceptional candidates, we will consider sponsoring visas and supporting relocation

• Compensation: competitive salary commensurate with experience

• Generous Benefits will be communicated in interviews

We are an Equal Employment Opportunity employer and do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable law or company policy. We strive for a erse, healthy and safe workplace and strictly prohibit harassment of any kind.

Title: Life Enrichment Assistant

Location: San Rafael United States

Part Time

Job Description:

Job Description

The Life Enrichment Assistant @ Drake Terrace is responsible for implementing and supporting aspects of the community's Art of Living Well philosophy and the multi-dimensions of Art of Living Well through interaction with residents, presenting classes and instruction, coordinating events, and assisting with transportation as needed. Assist in promoting a healthy, activity-enriched lifestyle for residents and associates.

This is a part time position, Sunday-Tuesday, 9am-5:30pm.

Pay range: $22-23/hr

Hiring bonus: $500

What will I do every day?

• Assist Life Enrichment Director to present programs that meet the emotional, intellectual, social, spiritual and vocational needs of the residents and staff
• Promote and monitor resident attendance and participation in all Art of Living Well programs
• Teach and facilitate programs as appropriate
• Monitor residents' well-being in a general way and report any changes in condition to the appropriate associate/department immediately
• Assist residents with requests as needed or find appropriate associate to assist
• Learn resident preferences for opportunities to provide exemplary customer service, exceed resident expectations and enhance resident satisfaction
• Implement a variety of group and inidual Art of Living Well programs that meet the varying needs of the residents and staff
• Respond to residents inidually to meet their Life Enrichment needs based on activity level, acuity, interests, and feedback
• Work with volunteers and community groups as needed to implement various programs and events
• Assist in setting up/tearing down Life Enrichment and community events as needed
• Work as part of the team within your department and across the community
• Perform function ability assessments and quality of life indexes for participants, as requested
• Assist with scheduling transportation as required
• Drive vehicles as necessary
• Support open and honest communication with and between all associates
• Represent the company PVBs and The Art of Living Well on a daily basis
• Maintain high standards of personal appearance and grooming, which includes wearing the proper uniform and name tag when working
• Look for ways to reduce costs and create efficiencies on a daily basis
• Ensure regulatory compliance and report any issues or concerns immediately
• Support continuous improvement
• Comply with company standards and regulations to encourage safe and efficient community operations
• Adhere to all regulations, laws and company standards, including the Associate Handbook
• Understand and support the community sales process
• Perform other related duties as required

What will I need to be successful in this role?

• Bring a smile to work every day
• Be a great team player
• High school graduate
• One to two years' experience in Life Enrichment programs (preferably with seniors)
• Background in different dimensions of Art of Living Well is beneficial
• Experience leading exercise classes and assisting with exercise equipment
• Basic competency in the use of multiple forms of technology, including: Microsoft Office applications, internet-based and custom applications
• Ability to work a flexible schedule, including evenings, weekends and holidays as needed

Special Requirements/Certifications I may need?

• Valid driver's license and proof of good driving record
• Commercial Driver's License or ability to obtain one within reasonable time of employment (as required)
• First Aid Certification

What's in it for me? (Great Question!)

• Competitive pay
• A free meal per shift
• Healthcare Benefits including Vision & Dental (Full-time only)
• Matching 401k (Full-time only)
• Paid Time Off
• Rewards and Bonus Opportunities
• Continuous Training and Growth Opportunities

What do we do?

We create a great place to live for our residents and a great place to work for our associates. Kisco Senior Living has been a dynamic, award-winning leader in the senior living industry for over 30 years.

All offers of employment are subject to satisfying our pre-employment process, which includes successfully passing a drug screen, a job specific-related physical, a TB test, and a background check. If selected for employment, the company will cover the cost of these pre-hire requirements

Kisco Senior Living is an Equal Opportunity Employer

Title: Bank Senior Theatre Assistant

Location: Leicester United Kingdom

Job Description:

JobID: 22377

Category:

JobSchedule: Part time

Posted Date: 2026-04-23T13:01:18+00:00

JobShift:

:

Bank Senior Healthcare Assistant | Theatres | Leicester | Competitive Rates | Ad-Hoc Shifts | Days |

Spire Leicester Hospital is looking for a highly motivated Healthcare Assistants to join their friendly theatre team on the bank, this is your opportunity to join one of the UK's leading private hospitals and take your career to the next level.

You will see a wide range of surgical patients within our hospitals including Gynaecology, Urology and Orthopaedics, ENT, Breast Surgery, Ophthalmology.

Duties and responsibilities:

• Assist the multi-disciplinary team in Theatres by providing an efficient and sensitive supporting role
• Be at the forefront of providing exceptional customer service to our valued patients, as you escort them between the wards, departments and theatre suites and deliver their meals
• Handling of equipment, medical records, specimens and line

Who we're looking for:

• An experienced, and preferably NVQ level 2/3 qualified, Healthcare Assistant / Support Worker
• Previous experience within a theatre environment is desirable however an acute hospital environment would be considered
• You will need to have a flexible attitude to work
• You will need outstanding communication skills, and you will be able to follow instructions precisely
• You will be experienced in supporting a variety of theatre specialities and you will be directly involved in patient care, communicating important information to teams in the anaesthetic room/theatre.

Benefits:

• Bank colleagues are paid weekly
• We offer competitive rates to our bank colleagues who work on a flexible basis, often to cover busy periods, sickness, or annual leave
• Unsocial Enhancements, dependent upon shift pattern worked (won't be applicable for all)
• Access to Spire Healthcare pension
• Access to Blue Light Card discounts
• Smart spending discounts (in addition to Blue Light discounts) via 'Spire for You'
• Wellbeing Centre access via 'Spire for You'
• Free uniform
• Free DBS
• Full induction, including mandatory training updates
• Opportunities for further training and progression into permanent posts
• Knowledge, support and guidance through your recruitment journey from Spire's specialist Resourcing Team
• We offer competitive rates to our bank colleagues who work on a flexible basis, often to cover busy periods, sickness or annual leave.

Our Values

We are extremely proud of our heritage in private healthcare and of our values as an organisation:

• Driving clinical excellence
• Doing the right thing
• Caring is our passion
• Keeping it simple
• Delivering on our promises
• Succeeding and celebrating together

Our people are our difference; it's their dedication, warmth and pursuit of excellence that sets Spire Healthcare apart.

We commit to our employee's well-being through work life balance, on-going development, support and reward.

"Spire Healthcare is a leading independent healthcare group in the United Kingdom, running 38 hospitals and over 50 clinics across England, Wales and Scotland. It provides diagnostics, inpatient, day case and outpatient care, operates a network of private GPs and provides workplace health services to over 800 corporate clients. It also delivers a range of private and NHS mental health, musculoskeletal and dermatological services."

For us, it's more than just treating patients; it's about looking after people.

If we have received sufficient applications, this date may be brought forward so please submit your application as soon as possible.

Title: Senior/Medical Science Liaison - PAH (Dallas/Houston)

remote type

Remote

locations

Dallas/Fort Worth, TX

Louisiana (Remote)

New Mexico (Remote)

Oklahoma (Remote)

time type

Full time

job requisition id

R04944

Job Description:

The job details are as follows:

Who We Are

We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.

United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter’s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).

The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.

Who You Are

You are a strategic thinker with a strong work ethic who enjoys supporting HCPs and other internal stakeholders across the organization. As a self-starter and team player, you combine initiative, nimbleness, and strong communication skills with positive energy to deliver results in a compliant manner. You are known for being easy to work with, embracing learning, and thriving in a collaborative and dynamic environment.

The Senior/Medical Science Liaison will serve as the primary field-based point of contact for current and future clinical investigators, speakers, and other health care providers on a range of clinical and scientific issues. Serve as a mentor/trainer for junior level MSLs, taking the lead on key Medical Affairs projects and providing leadership to the MSL team in the absence of the Senior Manager/Manager on a limited basis in the case of their absence.

• Respond to unsolicited requests for information that is beyond the scope of that which is approved for promotional use while adhering to United Therapeutics policy on the dissemination of scientific information
• Serve as the primary contact between PAH centers and internal departments (i.e. Medical Affairs / Clinical Operations) with regard to company and investigator-initiated studies, ensuring scientific validity and alignment with the company’s medical strategy
• Establish and maintain relationships with current and prospective thought leaders by engaging in discussions related to publication concepts and advisory boards and responding to grants request and CME educational endeavors
• Provide medical and scientific training and support to key internal stakeholders, including clinical research associates, field sales teams, and marketing teams
• Manage project work related to Medical Affairs activities as assigned by the senior management of Medical Affairs. This includes contributing to the development of departmental infrastructure (eg, drafting SOPs) and identifying opportunities to enhance departmental work stream efficiencies

Territory to include: TX, NM, OK, LA, MS

Minimum Requirements

Medical Science Liaison

• 6+ years of experience working in the biotech / pharmaceutical industry (or appropriate clinical setting) with a Master's Degree in life sciences or relevant field (e.g., NP, PA) or,
• 2+ years of experience working in the biotech / pharmaceutical industry (or appropriate clinical setting) with a PharmD, PhD, or MD and
• 3+ years of clinical experience in cardiovascular, respiratory, pulmonary or relevant disease state(s)
• 1+ years as a Medical Science Liaison or equivalent combination of clinical and MSL experience
• Ability to exhibit excellent verbal and written communication skills, including the effective conveyance of scientific and medical information to erse audiences, both internal and external, in various settings
• Strong team collaboration, planning, communication, and organizational skills
• Demonstrated ability to proactively drive initiatives and innovate solutions
• Proficient in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint)
• Strong presentation, facilitation and instructional skills
• Ability to travel up to 80%, including overnight travel

Minimum Requirements

Senior Medical Science Liaison

• 8+ years of experience working in the biotech / pharmaceutical industry (or appropriate clinical setting) with a Master's Degree in a relevant life sciences field (e.g., NP, PA) or,
• 5+ years of experience working in the biotech / pharmaceutical industry (or appropriate clinical setting) with a PharmD, PhD, or MD
• 3+ years of experience working in PAH
• 2+ years of experience working as a MSL
• Ability to exhibit excellent verbal and written communication skills, including the effective conveyance of scientific and medical information to erse audiences, both internal and external, in various settings
• Strong team collaboration, planning, communication, and organizational skills
• Demonstrated ability to proactively drive initiatives and innovate solutions
• Proficiency with Microsoft Excel, PowerPoint, and Word
• Expert level of scientific knowledge
• Strong presentation, facilitation and instructional skills
• Ability to travel up to 80%, including overnight travel

Preferred Qualifications

• Ability to work independently and adapt to changing work demand and new processes
• Demonstrated commitment to high standards of performance; adept at multitasking, prioritization, and results-oriented work

Position Location

This position is located remotely within the United States with ideal candidates living in TX, NM, OK, LA, MS

The salary range for this position is $140,000 - $220,000 and reflects our good-faith estimate of the compensation for this role at the time of posting. An employee’s position within the salary range will be based on factors such as education, qualifications, experience, skills, geographic location, and business needs, as well as other factors permitted by law at the time of posting. This range may be modified in the future based on company and market factors.

Eligible employees may participate in the Company’s comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off & paid parental leave benefits, disability benefits, and more.

United Therapeutics  Corporation is an Equal Opportunity Employer, including veterans and iniduals with disabilities.

Title: Strategy Insights & Planning Associate Consultant - Risk-Based Quality Management (RBQM)

Location: South San Francisco United States

Job Description:

• Insights & Analytics
• Strategy Insights & Planning
• $117,500.00 - $133,250.00
• 32743

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage and passion to drive life-changing impact to ZS.

What you’ll do: Strategy Insights & Planning Associate Consultant in the Insights & Analytics Capability Group will… 

ZS's Strategy Insights and Planning teams partner with clients to design and deliver solutions to help them tackle a broad range of business challenges. Our teams work on multiple projects simultaneously, leveraging advanced data analytics and problem-solving techniques. Our recommendations and solutions are based on rigorous research and analysis underpinned by deep expertise and thought leadership.   

What you’ll do 

• Leverage structured problem-solving frameworks to develop solutions to complex business challenges across pharmaceutical R&D, with a focus on Risk-Based Quality Management (RBQM) and clinical development strategy
• Support design and execution of RBQM frameworks, including identification of critical-to-quality factors, key risks, and mitigation strategies across clinical trial portfolios
• Assist in structuring and conducting market, clinical, and operational research to generate insights that inform trial design, quality strategy, and risk oversight
• Design and deliver custom analyses using tools like Excel, Access, Confirmit, and ZS proprietary platforms to support risk monitoring, portfolio oversight, and decision-making
• Contribute to the development of clinical and quality ecosystems, including centralized monitoring approaches and scalable platforms for trial oversight
• Synthesize and communicate insights to clients through clear, executive-ready presentations, with emphasis on quality, risk, and regulatory readiness
• Build client relationships and serve as a key point of contact on workstreams related to RBQM, quality strategy, and clinical transformation
• Support program management, including tracking risks, identifying issues, and driving mitigation strategies to ensure successful project delivery
• Mentor junior team members and contribute to capability building in RBQM, quality management, and R&D transformation

What you’ll bring: 

• Bachelor’s, Master’s, or PhD in a field with quantitative or analytical coursework such as business, economics, engineering, life sciences, or related disciplines
• 2–5 years of relevant professional experience, with prior consulting experience required, ideally in pharmaceutical, biotech, or clinical research settings
• Experience or familiarity with Risk-Based Quality Management (RBQM) and/or Quality Risk Management, including exposure to clinical trial quality, monitoring, or risk frameworks
• Understanding of clinical development processes and regulatory expectations 
• Strong analytical and problem-solving skills, with the ability to design custom analyses and translate data into actionable insights
• Ability to think strategically about clinical trial portfolios, including risk identification, oversight, and performance tracking
• Strong communication skills with the ability to engage both business and clinical stakeholders
• High attention to detail with a quality-focused mindset, including exposure to SOP-driven environments and audit readiness
• Self-starter with strong organizational skills, adaptability, and a collaborative, team-oriented approach
• Fluency in English 
• Client-first mentality 
• Intense work ethic 
• Collaborative spirit and problem-solving approach

How you’ll grow:

• Cross-functional skills development & custom learning pathways
• Milestone training programs aligned to career progression opportunities
• Internal mobility paths that empower growth via s-curves, inidual contribution and role expansions

Perks & Benefits:

At ZS, your growth matters. We offer a comprehensive total rewards package that supports your health and well‑being, financial future, time away, and professional development. With robust skills‑building programs, multiple career progression paths, internal mobility, and a deeply collaborative culture, you’ll have the opportunity to do meaningful work, expand your capabilities, and thrive as part of a global community. For details on total rewards in United States, visit ZS US office locations | Where we work | ZS.               

Hybrid working model:

We are committed to giving our employees a flexible and connected way of working.  A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections.

Travel:

Travel is a requirement at ZS for client facing ZSers; business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed.  Travel provides opportunities to strengthen client relationships, gain erse experiences, and enhance professional growth by working in different environments and cultures.

Considering applying?

At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems—the ones that comprise us as iniduals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are integral to your success here. We are committed to building a team that reflects a broad variety of backgrounds, perspectives, and experiences. Learn more about our inclusion and belonging efforts and the networks ZS supports to assist our ZSers in cultivating community spaces and obtaining the resources they need to thrive.

If you’re eager to grow, contribute, and bring your unique self to our work, we encourage you to apply.

ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law.

To complete your application:

NO AGENCY CALLS, PLEASE.

Title: Neurologist 

Location: Duluth, GA

Work Type: Hybrid, Full Time

Job ID:  2025-99437

Job Description:

Northside Hospital is award-winning, state-of-the-art, and continually growing. Constantly expanding the quality and reach of our care to our patients and communities creates even more opportunity for the best healthcare professionals in Atlanta and beyond. Discover all the possibilities of a career at Northside today.

Northside Hospital Duluth is seeking a Hybrid Neurologist to join a highly established outpatient practice and the Neurohospitalist team. This unique opportunity allows for autonomy and the ability to establish deep patient relationships within a supportive community.

As a nationally recognized leader in multiple specialties, Northside Hospital works to collaborate with the best of providers, to help us continue to advance our model of high-quality and compassionate care into the future with a passion for Excellence, Innovation, Community, and Teamwork. Northside Hospital's model of excellence is reflected in the recent awards including being names Forbes Best Companies and Best Places to Work.

Position Highlights

• Monday-Friday from 8:00 am to 5:00 PM
• No Hospital Call with this Hybrid Neurology Position
• Work both as a Neurohospitalist and an Outpatient Neurologist-Keep Up with All Your Skills
• Established Outpatient practice with a large catchment area
• High earning potential with production and quality bonuses
• Voted by Newsweek among America's Best in State Hospitals 2025.

Benefits Overview

• Incredible Retirement Benefits including a Fully Funded Pension Plan
• 457 Retirement Plan with Matching
• CME Allowance
• PTO
• Paid Malpractice
• Healthcare Benefits starting Day 1

Living in Gwinnett County:

• Excellent Schools: Gwinnett County is known for its top-rated public school system, which consistently ranks among the best in the state of Georgia. Families are drawn to the area for its quality education options and strong academic programs.
• Vibrant Communities: Gwinnett County is home to erse and vibrant communities, each with its own unique character and amenities. Residents can find neighborhoods ranging from bustling urban centers to peaceful suburban enclaves, offering something for everyone.
• Recreational Opportunities: The County boasts numerous parks, recreational facilities, and green spaces where residents can enjoy outdoor activities such as hiking, biking, picnicking, and sports. Gwinnett County also has several golf courses, sports complexes, and community centers for leisure and fitness activities.
• Cultural and Entertainment Options: Residents of Gwinnett County have access to a variety of cultural and entertainment venues, including theaters, museums, art galleries, and concert halls. The Gas South Arena is one of the most versatile venues, showcasing a multitude of concerts, sporting events, family shows, and more!

REQUIRED:

• MD/DO
• Board Eligible or Board Certified in Neurology
• Active or ability to obtain an active medical license in the state of Georgia
• Residency training in an accredited Neurology Program

Title: Nurse Case Manager - Fredericksburg, VA

Location:

Fredericksburg, VA 22401, USA•

Alexandria, VA, USA•

Dumfries, VA, USA•

Ashburn, VA, USA•

Chantilly, VA, USA

Req #1810

Job Description:

A Field Case Manager role is a field / home-based position with travel, up to 2 hours one-way (4 hours round trip), to doctors’ offices, hospitals, and various other locations.  This inidual is responsible for the medical case management of work-related injuries, which includes assessment, planning, coordination, implementation, and evaluation of injured/disabled iniduals. The Case Manager works with insurance carriers, medical care providers, attorneys, employers, and employees, and closely monitors the progress of the injured worker and reports results back to the employer and insurance carriers.  Must be willing to learn and take catastrophic cases. 

At Paradigm, People Come First

It's more than a job. It's a passion. Work at Paradigm, and you’ll find deep satisfaction knowing you’re making a profound difference in people’s lives.

• Meaningful work: better outcomes for all isn’t just our tagline. It’s what guides us to do our best—every day. At Paradigm, you’ll find an authentic connection between the work you do and your passion for making a difference in the world.
• Exceptional people: You'll work alongside smart people who share a commitment to excellence and a dedication to service. We're not here just for a "job." We're here to transform lives.
• Collaborative culture: At Paradigm, a spirit of collaboration and care is evident in everything we do. We promote a culture of inclusivity and value ersity of all kinds including thought, knowledge, and experience. No matter the team, everyone works together toward a common goal to deliver exceptional outcomes.

Qualifications:

• Current, unencumbered Registered Nurse (RN) license in VA
• Current, unencumbered Registered Nurse (RN) license in DC (required within 30 days of start date)
• Experience in case management of workers comp cases, preferred
  • Must be willing to learn and take catastrophic cases
• Recommended certifications (CCM, CRRN, CDMS, CRC) preferred.  REQUIRED within two years of the date of hire
• Skills required for success: organization and timeline adherence skills, PC and technology skills, communication skills (written, verbal, and interpersonal)
• Ability to operate autonomously with minimal oversight 
• Skilled at patient education 
• Valid Driver’s License, and good driving history

Paradigm Benefits:

• Health and wellness– We want our people to be and stay healthy, so we offer PPO, HDHP, and HMO health insurance options with Cigna and Kaiser (CA employees only).
• Financial incentives- Paradigm’s financial benefits help prepare you for the future: competitive salaries, 5% premium bonus paid over productivity requirements, premium pay for catastrophic files, cell phone and internet reimbursement, mileage reimbursement (federal rate), 401(k) matching contributions, employer-paid life and disability insurance, flexible spending, and employer-matched HSA contributions.
• Vacation - We believe strongly that work-life balance is good for you and for our company. We offer paid time off, paid holidays, and a personal holiday.
• Volunteer Time - We want our employees to engage with and give back to their communities in meaningful ways. Full and part-time employees receive one paid day per calendar year.
• Learning and development - One of Paradigm's core values is expertise, so we encourage our employees to continually learn and grow. We support this in a variety of ways from our Dedicated Training Department that offers an 8-12 week new hire onboarding program.

Paradigm believes that fostering a erse and inclusive workplace is central to our mission of helping more people and transforming lives. We’re striving to build a culture that better reflects the society we live in and empowers our team to deliver the highest levels of compassion and care to those we serve. For us, achieving this goal requires a workforce that respectfully embraces differences and commits to positive change, creating an environment where everyone is able to bring their whole self to work.

#LI-Hybrid

Job Family

Active

Pay Type

Salary

Travel Required

Yes

Hiring Min Rate

90,000 USD

Hiring Max Rate

99,000 USD

Title: Business Manager

, Practice Growth - New Jersey North, NJ

Location: Newark United States

Job Description:

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting inidual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace ersity and respect the dignity, privacy, and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Job Title: Aesthetic Business Manager (ABM), Practice Growth

Location: New Jersey North, NJ

Job Summary

The Aesthetic Business Manager (ABM), Practice Growth role serves as a strategic B2B sales overlay partner responsible for driving growth, elevating clinical adoption, and enhancing business performance across strategic accounts in the Aesthetics business space. This role supports field sales teams, aesthetic practices and HCPs by delivering expert product knowledge, targeted business development growth strategies, and practice optimization initiatives to increase market share and expand the utilization of Galderma Aesthetics products.

Key Responsibilities

• Promote and support the sales of Galderma Aesthetics products to targeted customers within a defined region, functioning as a strategic resource to complement Portfolio ABM sales roles.
• Own and achieve product specific revenue targets across assigned territories.
• Implement action plans to increase product penetration, expand market share, and accelerate account growth for Galderma aesthetics products in specific customer accounts and/or markets.
• Drive B2B product sales through the implementation and delivery of approved promotional items, approved field-based programs and educational events.
• Utilizes effective direct selling techniques and market strategies to expand product demand. Analyze market trends, competitive dynamics, and practice performance to uncover new growth pathways and strategically support the sales team.
• Develop and coordinate HCP training programs and practice enhancement in-services and open houses.
• Provide in-depth product and procedure expertise to healthcare providers and staff, helping them integrate aesthetic solutions confidently and effectively.
• Build strong, trust-based professional relationships with aesthetic providers, key decision-makers, and practice staff.
• Implement and execute key Marketing strategies.
• Maintains financial responsibility for all aesthetic sales transactions, ensuring accuracy, transparency, and compliance with organizational policies.
• Establish and maintain excellent communications and sound working relationships with co-workers and assigned physicians and healthcare providers.
• Ensures all aesthetic sales practices comply with regulatory, ethical, and organizational standards, including accurate pricing, documentation, and disclosure requirements.
• Actively participate in scheduled Company sales meetings, district and regional conference calls, business meetings, field rides, and ongoing training sessions.
• Demonstrate the highest levels of integrity and professionalism, adhering to all company policies, compliance standards, and industry regulations.
• Other duties as assigned.

Skills and Qualifications

• Minimum of 5+ years of proven B2B sales experience in quota-driven role; prior experience in dermatological, medical devices, specialty pharmaceutical sales, or capital equipment. Prior aesthetics experience highly preferred.
• Bachelor's degree from four-year college or university required.
• Demonstrated and sustained high performance throughout career.
• High sense of urgency regarding customer service with a strong customer focused mindset.
• Strong business acumen and ability to understand market opportunities with a strong aptitude for learning.
• Strong knowledge of the business and market in the assigned territory is preferred.
• Ability to travel is required by the specific territory.
• Ability to thrive in a highly driven culture that is performance based, fast paced, and results oriented.
• Must maintain a high degree of integrity and be highly ethical at all times.
• Drivers license required.

About the Compensation:

The base salary range for this role is determined based on several factors. These include but are not limited to job accountabilities; skill sets; experience and training; certifications; work location; competitive market rates and other business needs. At Galderma, it is not typical for an inidual to be hired at or near the top of the range for their role and compensation decisions are dependent on a unique combination of factors for each role. A reasonable estimate of the hiring range for this role is $90,000 - $130,000.

In addition to base salary, we provide an opportunity to participate in a competitive commission plan. We offer a competitive and comprehensive benefits program including health insurance, 401(k) plan with employer match, a generous paid time off policy, hybrid work schedules and more.

The pay range displayed above is the range of base pay is the range of base pay compensation within Galderma expects to pay for this role at the time of this posting.

What we offer in return

You will be working for an organization that embraces ersity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our erse customer base. You will also have access to a range of company benefits, including a competitive wage with shift differential, annual bonus opportunities and career advancement and cross-training.

Next Steps

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
• The next step is a virtual conversation with the hiring manager
• The final step is a panel conversation with the extended team

Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Employers' Rights:

This job description does not list all the duties of the job. You may be asked by your supervisors or managers to perform other duties. You will be evaluated in part based on your performance of the tasks listed in this job description. The employer has the right to revise this job description at any time. This job description is not an employment contract, and either you or the employer may terminate employment at any time, for any reason. In addition, reasonable accommodation may be made to enable iniduals with disabilities to perform the essential functions of this position.

Title: IT Applications Analyst II

(PACS) | IT Applications - Clinical | Durbin

Job Description:

Overview

Work Location: Hybrid role with a strong need for onsite support during the initial transition period.

Analyzes application requirements and designing solutions to improve system functionality. Collaborates with cross-functional teams to implement and test software applications, troubleshooting issues to maintain optimal performance, and documenting processes for user reference. Supports end-users through training and inquiry resolution, monitors application performance, and recommends efficiency improvements. Coordinates with vendors for software updates and assisting in the development and execution of deployment plans.

Responsibilities

Key Responsibilities:

• Analyze application requirements and design solutions to enhance system functionality
• Collaborate with cross-functional teams to implement and test software applications
• Troubleshoot system issues to maintain optimal performance and reliability
• Document processes, workflows, and procedures for user reference and system consistency
• Provide end-user support through training and timely resolution of inquiries
• Monitor application performance and recommend improvements to increase efficiency
• Coordinate with vendors on software updates and assist with deployment planning and execution

Qualifications

Minimum Qualifications:

• Minimum of two (2) years of experience in application support or application training
• Experience analyzing and supporting IT applications
• Strong skills in software testing, troubleshooting, and performance monitoring
• Ability to provide effective end-user training and support
• Experience coordinating with vendors for system updates and deployments
• Knowledge of application security standards and compliance requirements

Preferred Qualifications:

• Three (3) or more years of experience in application analysis, content build, or project management within the applicable application or Epic module
• Advanced experience supporting and optimizing IT applications in a healthcare environment
• Experience with system configuration, workflow analysis, and performance improvement initiatives

Title: Manager, Upstream Marketing

Location: Weston United States

Job Description:

Work Flexibility: Hybrid

Stryker's Upper Extremities ision is committed to facilitating superior outcomes for our Shoulder Arthroplasty customers. Our business prioritizes enhancing clinical outcomes, streamlining complex procedures, and driving innovation through the adoption of advanced, industry-leading technologies.

In this role, the Manager, Upstream Marketing will be responsible for managing programs within our growing portfolio of enabling technologies for Shoulder Arthroplasty.

This position is based in our Columbia City, IN, Bloomington, MN, or Weston FL, with a hybrid occasional work from home flexibility. In this role, you will be required to travel up to 40% to domestic and international destinations.

What you will do

• Develop, maintain, and leverage erse networks for staying informed about competition.

• Understand market positioning and strengths/weaknesses of key competitors.

• Clearly articulate the value proposition to key stakeholders.

• Surface new or unexpressed customer needs, leading to enabling technology program enhancements.

• Identify new customer groups and tailors marketing strategies to meet both current and prospective customer needs.

• Focus product and service features and functions on the customer's critical success factors.

• Prepare and delivers program updates to Upper Extremities leadership team: business reviews, marketing strategies, proposals, and recommendations.

• Drive collaboration with global marketing teams to define enabling technology strategies.

• Lead the NPI process from start to finish, engaging key isional and enterprise stakeholders (R&D, finance, sales, operations, etc.) along the way.

• Demonstrate ability of sales forecasting methods and tools.

• Demonstrate ability to develop a pricing approach consistent with the marketing strategy and brand positioning.

• Accurately forecasts resource needs, including staffing and project expenses.

• Create Project Charters, CERs, and Business Case Financial Models as applicable.

• Develop personal relationships with surgeon key opinion leaders, strengthening engagement, collaboration, and alignment with the upper extremities business.

• Propose objectives for clinical evidence generation and evaluates inidual studies for alignments with evidence generation strategy.

• Other key attributes:

• Responsible and accountable for actions promoting an environment that fosters personal growth and development.

• Hold self to deliver high quality results with passion, energy, and drive to meet business priorities.

• Mentor, develops, and inspires others.

• Collaborate and influence others on cross-functional teams, advancing partnerships to achieve business objectives.

Required

• Bachelor's degree

• 8+ years of work experience

• Medical device marketing or sales experience

• New product development experience

• Partner or collaborating with R&D and other cross-functional businesses

• Excellent presentation and interpersonal communication skills

• Experience with executive-level presentations - great story-telling abilities

• Experience building compelling presentations and dashboards

• Business Case Financial Models

Preferred

• MBA

• Demonstrated proficiency in Microsoft Office (Excel, Word & PowerPoint)

• Professional experience in clinical settings and operating room environments

• Previous experience with shoulder arthroplasty or enabling technologies.

• Upper Extremities experience is a plus

• Enabling technologies, surgical navigation or robotics is a plus

• Working with Shoulder or Mako experience is highly desirable

United States of America Pay Ranges:

• USN: $118,000 - $196,700 USD Annual
• US5: $123,900 - $206,500 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 40%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to iniduals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

Title: Pharmacist

(RPh)- Work from Home, No Weekends

Location: Brooks United States

Job Description:

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Job Details

At our pharmacy, you will join a highly collaborative team of exceptional pharmacists who take pride in clinical quality, operational excellence, and doing what is right for patients. This role is intentionally focused on clinical work from home with a requirement to be dually licensed as a pharmacist in California and Kentucky.

Your time will be spent working from home providing pharmacist review and patient support between 8:00 AM and 8:00 PM EST. In this capacity, you will review prescriptions and patient medical history for appropriateness, help identify and resolve clinical or administrative issues, and provide counseling to patients and caregivers with professionalism and empathy and serve as the PIC (pharmacist-in-charge) for the state of California.

Work Location / Onsite Requirement

• Kentucky

Work Arrangement

• Remote: 100%

Licensure Requirements

• Required: Kentucky RPh license in good standing

• Required: California RPh license in good standing

Experience Requirement

• Required: Minimum 2 years in the practice of pharmacy

Facility / Hours

• Facility type: Closed-door specialty mail order pharmacy

• No weekends or holidays

Experience and Educational Requirements:

• Unrestricted Kentucky state and California state license as a Registered Pharmacist is required.

• Requires 2-3 years of directly related and progressively responsible experience.

• Degree in Pharmacy from an accredited College of Pharmacy is required.

Minimum Skills, Knowledge and Ability Requirements:

• Ability to communicate effectively both orally and in writing

• Ability to work quickly and accurately under time and volume constraints

• Strong leadership skills

• Strong interpersonal skills

• Ability to resolve customer issues quickly and creatively in order to improve customer satisfaction

• Familiarity with pharmaceutical products, services and drug interactions

• Strong organizational skills; attention to detail

• Good analytical skills

• Knowledge of Microsoft Word, Excel, PowerPoint and Outlook

What Cencora offers

We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit https://www.virtualfairhub.com/cencora

Full time

Equal Employment Opportunity

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company's continued success depends on the full and effective utilization of qualified iniduals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to iniduals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [email protected]. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned

Affiliated Companies

Affiliated Companies: Cencora Patient Services, LLC

Business Change Director

Location:

VA-RICHMOND, 2015 STAPLES MILL RD,

CA-WOODLAND HILLS, 21215 BURBANK BLVD

CA-COSTA MESA, 3080 BRISTOL ST, STE 200

MD-HANOVER, 7550 TEAGUE RD, STE 500

IN-INDIANAPOLIS, 220 VIRGINIA AVE

View Fewer Locations

locations

FL-MIAMI, 11430 NW 20TH ST, STE 300

OH-MASON, 4361 IRWIN SIMPSON RD

OH-SEVEN HILLS, 6000 LOMBARDO CENTER, STE 200

CA-WALNUT CREEK, 2121 N CALIFORNIA BLVD, 7TH FL

IL-CHICAGO, 8600 W BRYN MAWR AVE, 10th & 11th FL

WA-SEATTLE, 705 5TH AVE S, STE 300

IL-CHICAGO, 233 S WACKER DR, STE 3700

GA-ATLANTA, 740 W PEACHTREE ST NW

NJ-ISELIN, 111 S WOOD AVE, STE 220

FL-LAKE MARY, 3200 LAKE EMMA RD, STE 1000

OH-COLUMBUS, 8940 LYRA DR, STE 300

FL-TAMPA, 5411 SKY CENTER DR

VA-ROANOKE, 602 S JEFFERSON ST

VA-NORFOLK, 5800 NORTHAMPTON BLVD

Job Description:

Anticipated End Date:

2026-05-02

Position Title:

Business Change Director - Epic Systems

Job Description:

Business Change Director - Epic Systems

Hybrid 2: This role requires associates to be in-office 3 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. Alternate locations may be considered if candidates reside within a commuting distance from an office.

Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law.

The Business Change Director - Epic Systems is responsible for specializing in Epic Systems integration and data exchange initiatives, ensuring alignment between business objectives, system capabilities, and enterprise strategy.

This Director will ensure seamless, secure, and accurate data exchange, troubleshooting interface errors, and collaborating with technical teams for optimal system integration and performance. In addition, assist with designs, configures, tests, and maintain data interfaces (HL7, FHIR) between the Epic EHR system and external applications.

How You Will Make an Impact

Primary duties may include, but are not limited to:

• Specializes in and directly supports Epic Payer Platform integration initiatives, ensuring activities are aligned with corporate strategy and enterprise data objectives.

• Identifies potential issues, project changes, and scope data, including risks and impacts related to Epic system integrations and data exchange workflows.

• Leads efforts to identify best practices in process improvement, system integration governance, testing coordination, and release readiness for Epic-related initiatives.

• Identifies impacted parties, business partners, and resources required, including Epic application teams, integration teams, operational stakeholders, and external partners.

• Develops and designs processes and systems that support business needs, including Epic integration workflows, data exchange coordination, and cross-functional alignment models.

• Designs methods for integrating functions and processes, including oversight of Epic EHR interface strategies (e.g., HL7/FHIR integrations) and cross-team validation practices.

• Conducts cost/benefit analyses for integration enhancements, system improvements, and Epic upgrade initiatives.

• Builds support for business change throughout the business unit by partnering with Epic users, operational leaders, and data stakeholders to promote adoption and data quality improvements.

• Provides process, project, and change management methodology coaching/consulting support to both local and enterprise-wide initiatives, including Epic upgrades and integration-related enhancements.

• Leads project prioritization and scheduling activities for the business unit, including Epic integration initiatives, enhancements, and release milestones.

• Provides expertise to business areas in culture/change management activities and in process planning and portfolio management related to system integration efforts.

• Supports the execution of the operating plan, including oversight of Epic-related initiatives, coordination of testing and validation activities, and monitoring progress against integration deliverables.

• Actively participates in Epic Payer Platform governance and cross-functional meetings to ensure alignment with enterprise data and business objectives.

Minimum Requirements:

Requires a BA/BS in a related field and minimum of 10 years managing mid to large-scale change/project initiatives; or any combination of education and experience which would provide an equivalent background.

Preferred Skills, Capabilities, & Experiences:

• Epic interoperability/integration experience, including Epic Bridges and/or related modules (e.g., Care Everywhere, HIM as applicable) strongly preferred.

• Experience designing, configuring, testing, and supporting Epic interfaces and data exchange (e.g., HL7 and/or FHIR), including troubleshooting, error remediation, and Work Queue maintenance strongly preferred.

• Experience with interface-related message and data formats such as HL7, XML, X12, and common healthcare transactions/workflows (e.g., Admissions Discharge Transfer (ADT), appointments, authorizations/prior authorization) strongly preferred.

• Experience partnering with operational and technical stakeholders to document data requirements and validate end-to-end testing, data quality, and release readiness (including quarterly release notes review and upgrade impacts) strongly preferred.

• Ability to develop basic operational reporting (e.g., status reporting; Epic reporting tools such as Reporting Workbench a plus) preferred.

• Experience and/or knowledge of Clinical Workflow preferred.

• Strong communication, organizational, and reporting skills preferred.

For candidates working in person or virtually in the below location(s), the salary* range for this specific position is $115,360.00 to $207,648.00

Locations: California; Columbus, OH; Illinois; Maryland; New Jersey; and Washington State

In addition to your salary, Elevance Health offers benefits such as a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). The salary offered for this specific position is based on a number of legitimate, non-discriminatory factors set by the Company. The Company is fully committed to ensuring equal pay opportunities for equal work regardless of gender, race, or any other category protected by federal, state, and local pay equity laws.

• The salary range is the range Elevance Health in good faith believes is the range of possible compensation for this role at the time of this posting. This range may be modified in the future and actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Even within the range, the actual compensation will vary depending on the above factors as well as market/business considerations. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, paid time off, stock, or any other form of compensation and benefits that are allocable to a

particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Job Level:

Director Equivalent

Workshift:

Job Family:

BSP > Business Support

Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health.

Who We Are

Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.

How We Work

At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business.

We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few.

Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process.

The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws.

Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact [email protected] for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Prospective employees required to be screened under Florida law should review the education and awareness resources at HB531 | Florida Agency for Health Care Administration.

NOTE: Workday keeps job postings active through 11:59:59 PM on the day before the listed end date. Example: If the end date is 3/13, the posting will automatically come down on 3/12 at 11:59:59 PM. In other words - the job is posted until 3/13, not through 3/13.

Title: Clinical Recruiter

(Remote)

Location: United States

Job Description:

Description & Requirements

Join our team as a Clinical Recruiter and play a vital role in connecting top healthcare talent with meaningful opportunities. This work-from-home position offers the chance to collaborate with a dynamic, mission-driven team supporting a wide range of clinical healthcare programs and contracts. We are seeking a motivated professional with a strong understanding of clinical roles and healthcare environments who thrives in a fast-paced, high-impact setting.

In this role, you will partner closely with hiring managers and program leaders to identify, attract, and hire qualified clinical professionals across multiple specialties. Your expertise in healthcare recruiting and ability to build strong candidate relationships will directly contribute to the success of critical programs and the delivery of quality care. If you are passionate about making a difference, enjoy working remotely, and bring clinical healthcare experience or recruiting expertise, we encourage you to apply and grow your career with Maximus.

Why Maximus?

• Work/Life Balance Support - Flexibility tailored to your needs!
• Competitive Compensation - Bonuses based on performance included!
• ️ Comprehensive Insurance Coverage - Choose from various plans, including Medical, Dental, Vision, Prescription, and partially funded HSA. Additionally, enjoy Life insurance benefits and discounts on Auto, Home, Renter's, and Pet insurance.
• Future Planning - Prepare for retirement with our 401K Retirement Savings plan and Company Matching.
• ️Unlimited Time Off Package - Enjoy UTO, Holidays, and extended sick leave, along with Short and Long Term Disability coverage.
• Holistic Wellness Support - Access resources for physical, emotional, and financial wellness through our Employee Assistance Program (EAP).
• Recognition Platform - Acknowledge and appreciate outstanding employee contributions.
• Tuition Reimbursement - Invest in your ongoing education and development.
• Employee Perks and Discounts - Additional benefits and discounts exclusively for employees.
• Maximus Wellness Program and Resources - Access a range of wellness programs and resources tailored to your needs.
• Professional Development Opportunities-Participate in training programs, workshops, and conferences.
• Licensures and Certifications-Maximus assumes the expenses associated with renewing licenses and certifications for its employees.

Essential Duties and Responsibilities:

• Performs key sourcing and recruiting duties to hire qualified clinical professionals for a range of positions, including nursing, allied health, clinical research, and other healthcare-related roles. Iniduals in this role manage the full recruitment lifecycle for clinical positions.
• Screens, interviews, and assesses candidates to determine qualifications, experience, and cultural fit for clinical positions.
• Provides guidance and support to hiring managers throughout the recruitment process.
• Manages the full recruiting lifecycle for clinical positions, from sourcing to offer negotiation, ensuring timely and efficient hiring.
• Sources and recruits qualified clinical professionals for a range of positions, including nursing, allied health, clinical research, and other healthcare-related roles.
• Builds and nurtures a pipeline of both active and passive candidates.
• Develops and implements targeted sourcing strategies aimed at identifying top clinical talent, using multiple channels such as job boards, social media, professional networks, and industry events.
• Collaborates with leadership to develop effective clinical recruitment strategies, ensuring that the right candidates are sourced and hired for various clinical roles within the organization.
• Builds and maintains strong relationships with both internal stakeholders and external candidates to foster long-term partnerships and ensure a steady flow of qualified candidates.
• Tracks and reports on key recruitment metrics, ensuring that all hiring activities align with organizational objectives and compliance requirements, including relevant healthcare regulations.
• Maintains accurate records in the applicant tracking system (ATS) and ensures proper documentation for all recruitment activities.

Minimum Requirements

• Bachelor's degree in relevant field of study and 3+ years of relevant professional experience required, or equivalent combination of education and experience.
• Bachelor's degree or equivalent experience, with 3+ years of clinical or healthcare recruiting experience.
• Proven experience managing full-life cycle recruitment for clinical roles (e.g., nursing, allied health, clinical research).
• Demonstrated ability to source and engage both active and passive candidates using erse channels (job boards, social media, networking, etc.).
• Experience partnering with hiring managers and stakeholders to support hiring decisions and recruitment strategies.
• Strong candidate assessment skills, including screening and interviewing for qualifications and cultural fit.
• Familiarity with applicant tracking systems (ATS) and maintaining accurate recruitment data and documentation.
• Knowledge of healthcare recruiting practices and applicable compliance considerations.
• Excellent communication, organization, and relationship-building skills.
• Ability to manage multiple priorities in a fast-paced, dynamic environment.
• Ability to work independently in a remote or distributed team environment.

Preferred Skills and Qualifications

• Experience using the Avature Applicant Tracking System (ATS) to manage full-cycle recruiting activities, including candidate pipeline development, interview coordination, and reporting.
• Proficiency with Smartsheet for tracking recruiting metrics, managing workflows, and supporting project coordination across multiple programs.
• Experience with high-volume, contract, or time-sensitive recruiting environments (e.g., bids, proposals, ramps, etc.).

Home Office Requirements

• Maximus provides company-issued computer equipment
• Reliable high-speed internet service
• Minimum 20 Mpbs download speeds/50 Mpbs for shared internet connectivity
• Minimum 5 Mpbs upload speeds
• Private and secure workspace

EEO Statement

Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics.

Pay Transparency

Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off. Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances.

Accommodations

Maximus provides reasonable accommodations to iniduals requiring assistance during any phase of the employment process due to a disability, medical condition, or physical or mental impairment. If you require assistance at any stage of the employment process-including accessing job postings, completing assessments, or participating in interviews,-please contact People Operations at [email protected].

Title: Senior Structural Engineer 

Kiewit Power Engineering Group

Location: Raleigh United States

Job Description:

Requisition ID: 180482

Job Level: Senior Level

Home District/Group: Kiewit Power Engineering

Department: Design Engineering

Market: Power

Employment Type: Full Time

Position Overview

As a Structural Design Engineer, you will be a part of a growing team that supports all aspects of the construction process by performing innovative design engineering through brainstorming conceptual designs, performing and/or reviewing structural calculations, developing plans, scheduling tasks to meet client needs, as well as mitigating risk to keep our construction crews safe.

District Overview

Kiewit Power Engineers brings various project types to life across North America, including gas-fired generation, power delivery, environmental retrofits, renewables and new technology, and water/wastewater. Our staff leads the power markets engineering process and collaborates with Kiewit's construction teams to focus on safe, cost-effective and innovative designs that achieve client expectations and further Kiewit's legacy of excellence.

Location

This position can be based in any of the following office locations: Lenexa, KS; Houston, TX; Raleigh, NC; or Phoenix/Tempe, AZ.

For roles in Chattanooga, TN; Detroit, MI; or Richmond, VA, the position will start remotely and transition to a hybrid/in office arrangement once the new office is established.

Responsibilities

• Develops and checks less experienced engineers to solve design issues.
• Identifies alternate solutions that relates to quality and best cost options.
• Generates solution strategies that allow use of others to work toward the solution.
• Interacts effectively with other groups to find best solutions to complex issues.
• Reviews and corrects the work of engineers and designers developing engineering and design documents as needed for the project.
• Provides resolutions for technically complex issues.
• Develops mid to major-sized project or proposals with no supervision.
• Leads others in project objectives consistent with that of the organization.
• Considers multiple solutions and makes good decisions based on good data analysis.
• Manages several different assignments simultaneously.
• Creates innovative working methods to generate new ideas.
• Uses resources to identify new solutions and finds best cost solutions.
• Serves as resource to less experienced engineers.
• Reviews application of standards for correct interpretation.
• Leads projects in how to interpret and apply codes and standards.
• Leads team to identify changes in the scope of work during large-sized projects.
• Produces design changes as needed to stay within budget and schedule.
• Recognizes the importance of customer needs.
• Performs and leads quality checks of the design and engineering of major-sized project to ensure accuracy.
• Plans work independently with no supervision and consults others on technical details of their work.

Qualifications

• Bachelor's degree in Civil Engineering minimum required.
• 10 - 20 years' minimum relevant experience in Industrial or the Power Generation industry.
• Acts independently to determine methods and processes for assignments.
• Trains and leads team of engineers as needed.
• Leads team for work with high complexity.
• Work with project team as representative and coordinates work within discipline department.
• Adjusts to varying demands of work and performs well.
• Develops and presents work in well-constructed written and verbal presentations. Clearly conveys messages and ideas, gains understanding.
• Communicates effectively across all departments of organization.
• Works collaboratively across departments and with field to solve problems.
• Initiates meetings within own team, other disciplines or internal customers for clarity on work.
• Supports project teams and departments in a positive and productive manner. Works well with other to accomplish common goals and objectives.
• Serves as technical resource to engineers, designers and other departments.
• Continuously looking for ways to improve processes for customers and makes recommendations for improvements.

#LI-PC1

Working Conditions

Other Requirements:

• Regular, reliable attendance
• Work productively and meet deadlines timely
• Communicate and interact effectively and professionally with supervisors, employees, and others inidually or in a team environment.
• Perform work safely and effectively. Understand and follow oral and written instructions, including warning signs, equipment use, and other policies.
• Work during normal operating hours to organize and complete work within given deadlines. Work overtime and weekends as required.
• May work at various different locations and conditions may vary.

We offer our fulltime staff employees a comprehensive benefits package that's among the best in our industry, including top-tier medical, dental and vision plans covering eligible employees and dependents, voluntary wellness and employee assistance programs, life insurance, disability, retirement plans with matching, and generous paid time off.

Equal Opportunity Employer, including disability and protected veteran status.

Title:  Mental Health Therapist

- Plano

Location: Coit/Plano United States

Job Description:

Geode Health is a rapidly growing, national provider of outpatient mental health services. Our Mission is to "Transform mental health by making it more accessible, affordable and effective".

We are actively recruiting for a passionate Licensed Mental Health Therapist in the greater Plano market who can partner with us to achieve that mission. As a Geode Health Therapist you will diagnose and treat mental health disorders and do psychotherapy across the general spectrum of mental healthcare conditions. You will help people define goals, gain insights all through personalized committed care. You will collaborate with other healthcare professionals to provide care coordination, providing crisis intervention if needed.

Voted "Best Places to Work" in 2025 by Glassdoor.com

Things our Mental Health Therapist enjoy at Geode:

Flexibility to create your own schedule.

You can create your own work schedule. We do need that in advance and expect full-time hours, but you get to design when you are available for booking. We offer after hours urgent support to give you a lifestyle you deserve, too.

Hybrid work schedule.

Most of our Mental Health Therapist work three days a week onsite and two days a week telehealth. It is reasonable to expect you may do more in-person time up front, while you build up your patient case load and schedule follow ups on telehealth days.

Our model is working. Our patients like it too.

We are an organization that employs evidence-based care and have a proven model that is significantly improving the lives of the vast majority of our patients. Our providers use a measurement-based care approach, which allows them to track outcomes through data to inform their plan of care, so they can strive to provide best-in-class psychiatric/therapeutic care.

Check out our Google reviews - we think you will find our patients like it too.

Integrated care team.

You will be part of a team of dedicated mental health providers who all work together as colleagues to focus on providing great care. As a mental health therapist, you will partner with the Provider so the full spectrum of psychiatric and therapeutic care is well coordinated. Together, moving patients up and down the care continuum, as needed.

We invest in you, too.

• Competitive compensation, no earnings cap
• Quality incentive bonus
• Professional development, CME reimbursement
• Medical, Dental, Vision, 401k match
• Marketing support, we partner with you to fill your patient case load
• Spacious, beautifully designed modern office
• Administrative support

This Mental Health Therapist role requires:

• Active license (LCSW, LPC or LMFT) in the state of Texas
• Passion for high quality care
• Experience conducting comprehensive assessments of clients and developing inidualized treatment plans
• Proficiency in using an EMR system and ensuring accurate and up to date electronic health records for all patient encounters
• Understanding of mental health disorders and treatment modalities
• Desire and ability to see a general spectrum of mental health conditions. We believe everyone deserves access to care
• Geode prefers Therapist who have over one year of professional experience doing psychotherapy

Title: Public Health Program Nurse

Location: Buffalo United States

locations

Buffalo, NY

time type

Full time

posted on

Posted 5 Days Ago

time left to apply

End Date: May 5, 2026 (9 days left to apply)

job requisition id

JR-0002104

Applications to be submitted by May 04, 2026

Compensation Grade:

P24

Compensation Details:

Minimum: $95,130.00 - Maximum: $95,130.00 Annually

Positions with a designated work location in New York City, Nassau, Rockland, Suffolk, or Westchester Counties will receive a $4,000 annual downstate adjustment (pro-rated for part-time positions).

Department

(OPH) Office of Public Health

Job Description:

Responsibilities

The Public Health Program Nurse (PHPN) will work to improve the health of Western New York communities by providing training, technical assistance, resources, guidance, and clinical guidance on community health services to local health departments, community-based organizations, and other community partners within the 17 counties of Western New York.  The PHPN will monitor public health data, contribute to the identification of public health issues, contribute to strategies to promote health equity programming, and evaluate activities implemented. The PHPN will facilitate enhanced collaboration and coordination between Community Health programs, providers, and other key stakeholders to improve health outcomes for infants, children, adolescents, and adults.  The PHPN will work to improve the health of communities by providing training, technical assistance, resources, guidance, and clinical guidance to local health departments, community-based organizations, and other community partners regarding health education and health promotion activities including implementation of the Prevention Agenda and implementation of the Chronic Disease Action Plan.  The PHPN may participate in public health emergency response activities as needed.

Minimum Qualifications

A Bachelor’s of Science degree in Nursing AND a license and current registration as a professional registered nurse in NYS AND four years of experience planning, evaluating, or administering health services or teaching in a health related program; OR an Associate’s degree in Nursing AND a license and current registration as a professional registered nurse in NYS AND six years of experience planning, evaluating, or administering health services or teaching in a health related program.  A Master’s degree in nursing may substitute for one year of experience planning, evaluating, or administering health services or teaching in a health related program.

Preferred Qualification

Familiarity with family health and/or chronic disease activities including maternal, child, and reproductive public health services; and prevention and control activities related to cancer, diabetes, cardiovascular disease, and/or asthma. Experience in oversight and evaluation of public health and preventive health programs, as well as promoting public health messages. Experience supervising staff. Experience managing multiple tasks, developing, and delivering educational materials, coordinating training activities, and contributing on policy development. Excellent organizational, interpersonal, and written and oral communication skills. Proficiency with computer-based software packages such as Microsoft Office, Outlook, etc.

Conditions of Employment

Grant funded position. Compliance with funding requirements such as time and effort reporting, grant deliverables, and contract deliverables, is required.

Valid and unrestricted authorization to work in the U.S. is required. Visa sponsorship is not available for this position.

Travel up to 25% of the time will be required.

The selected candidate must reside within a reasonable commuting distance of the official work location specified in the job posting and must also be located in or willing to relocate to one of the following states: New York, New Jersey, Connecticut, Vermont, or Massachusetts, prior to hire.

This position is eligible for a hybrid work schedule, with a combination of onsite and remote work.

HRI participates in the E-Verify Program.  

Affirmative Action/Equal Opportunity Employer/Qualified Iniduals with Disabilities/Qualified Protected Veterans

www.healthresearch.org

About Health Research, Inc.

Join us in our mission to make a difference in public health and advance scientific research! At Health Research, Inc. (HRI), your work will contribute to meaningful change and innovation in the communities we serve! At HRI, we are on a mission to transform the health and well-being of the people of New York State through innovative partnerships and cutting-edge public health initiatives. As a dynamic non-profit organization, HRI plays a crucial role in advancing the strategic goals of the New York State Department of Health (DOH), Roswell Park Comprehensive Cancer Center (RPCCC), and other health-related entities.

HRI offers a robust, comprehensive benefits package to eligible employees, including:

• Health, dental and vision insurance - Several comprehensive health insurance plans to choose from;

• Flexible benefit accounts - Medical, dependent care, adoption assistance, parking and transit;

• Generous paid time off - Paid federal and state holidays, paid sick, vacation and personal leave;

• Tuition support - Assistance is available for iniduals pursuing educational or training opportunities;

• Retirement Benefits - HRI is a participating employer in the New York State and Local Retirement System and offers optional enrollment in the New York State Deferred Compensation Plan. HRI provides a postretirement Health Benefits Plan for qualified retirees to use towards health insurance premiums and eligible medical expenses;

• Employee Assistance Program - Provides educational and wellness programs, training, and 24/7 confidential services to assist employees, both personally and professionally;

• And so much more!

Work Location Expectations

At HRI, the nature of hybrid and onsite work varies by position. Some roles require full onsite presence, while others allow a hybrid schedule. Managers determine the specific telecommuting expectations for each role based on operational needs and job responsibilities. If designated as hybrid, you will ide your time between working remotely and reporting onsite. Regardless of telecommuting status, all HRI employees must live within a reasonable commuting distance of their official work location and must reside in one of the following states: New York, New Jersey, Connecticut, Massachusetts, or Vermont.

Job Description: Membership Sales Manager

- Sun City West, AZ

Location: Hybrid (90% field‑based within the market; 10% remote)

Candidate must live within 50 to 75 miles of Sun City West, AZ.

This territory includes the following counties: Yavapai and West Maricopa.

On Target Earnings: $75,785.28 - $180,000

Two fixed base salary options are available, $35,000 or $45,000 (non‑negotiable).

Includes Car Allowance and Uncapped Commission

We are seeking a dynamic, community‑focused Membership Sales Manager to generate leads and sales for our AirMedCare Network membership through local B2C and B2B channels. This role is highly visible within the community and ideal for someone who enjoys building trusted relationships with residents, business owners, and community organizations throughout Sun City West and the surrounding counties.

Through consistent local engagement, you will develop a strong pipeline of new membership opportunities while supporting both inidual territory goals and broader team objectives. The ideal candidate brings a consultative sales approach, thrives in a relationship‑based environment, and understands the importance of service, trust, and peace of mind are especially important to this market.

AirMedCare Network (AMCN) is part of Global Medical Response (GMR) the largest medical transportation company in the world. AMCN delivers compassionate, quality medical care, primarily in the areas of emergency and patient relocation services across the United States. We offer unique membership programs including emergent air, Fly‑U‑Home, and ground ambulance services, providing critical coverage and reassurance to members and their families.

Responsibilities:

Drive Local Impact: Spend approximately 90% of your time in the field, engaging with local businesses (approximately 70% B2B) and inidual consumers (30% B2C) to promote AMCN membership programs throughout Sun City West and the surrounding communities.

Develop Relationships: Proactively identify and cultivate new leads through community events, local partnerships, cold calling, referrals, homeowner associations, senior‑focused organizations, and networking opportunities.

Sales Process Management: Navigate the full sales cycle from initial contact through enrollment, using a consultative, educational approach that addresses the unique needs of residents, families, and business partners in the territory.

Champion with Purpose: Act as a local brand ambassador by participating in health fairs, community meetings, local business events, and outreach opportunities, strengthening trust and awareness within the community.

Qualifications:

Education: High school diploma (or equivalent), valid driver's license, and a clean driving record.

Sales Expertise: Minimum 3 years of previous B2C or B2B field sales experience, including cold calling and active prospecting, preferred.

Industry Knowledge: Working knowledge of healthcare services, insurance products, or emergency medical transportation is preferred.

Community Orientation: Demonstrated ability to build long‑term relationships and successfully engage with community‑based audiences.

Why Choose GMR

Global Medical Response (GMR) and its family of solutions are dedicated to delivering compassionate, quality medical care, primarily in the areas of emergency and patient relocation services. Here, you'll embark on meaningful work that makes a real impact-both for you and for the communities we serve. View our employees' stories on how we provide care to the world at www.AtaMomentsNotice.com.

GMR's Core Behaviors-keep care at the center, raise your hand, seek to understand, find a way together and be accountable-unite our teams and set us apart in emergency medical services.

EEO Statement

Global Medical Response and its family of companies are an Equal Opportunity Employer, which includes supporting veterans and providing reasonable accommodations for iniduals with a disability.

Check out our careers site benefits page to learn more about our benefit options.

R0052167

Title: Manager Care Management Registered Nurse

/ RN

Division

Emory Univ Hosp-Midtown

Campus Location

Atlanta, GA, 30308

Campus Location

US-GA-Atlanta

Department

EHM Care Management

Job Type

Regular Full-Time

Job Number

158466

Job Category

Care Management

Schedule

8a-4:30p

Standard Hours

40 Hours

Hourly Minimum

USD $57.62/Hr.

Hourly Midpoint

USD $66.79/Hr.

Overview

Be inspired. Be rewarded. Belong. At Emory Healthcare.

At Emory Healthcare we fuel your professional journey with better benefits, valuable resources, ongoing mentorship and leadership programs for all types of jobs, and a supportive environment that enables you to reach new heights in your career and be what you want to be. We provide:

• Comprehensive health benefits that start day 1
• Student Loan Repayment Assistance & Reimbursement Programs
• Family-focused benefits
• Wellness incentives
• Ongoing mentorship, development, and leadership programs...and more!

Description

The Manager, Care Management (CM) is responsible for direct oversight of the daily operations of the Care Management department as it relates to Discharge Planning. Ensures departmental day to day operations are successful by creating schedules, arranging coverage, and iding work as necessary in order to ensure work is completed in a timely manner which will ensure compliance with regulatory requirements. Primary duties and responsibilities: Leadership and Management: 1. Responsible for maintaining and managing processes as it relates to day-to-day workflow. 2. Responsible for coaching, developing, training, and the performance management process for employees. 3. Ensures that department, ision, and system strategic goals are connected to the daily work of the department. 4. Understands metrics such as LOS, avoidable days, readmissions, saved days and will be able to implement measures in order to achieve targeted goals Collaboration and Communication: 1. Thorough ability to effectively communicate and organize workflow, must quickly and effectively break down barriers to discharge. 2. Works with Care Management Leadership and Physician Advisors across the system and will collaborate with the interdisciplinary teams as well as the revenue cycle teams as needed. 3. Displays a broad understanding of complex discharge planning and strength in problem solving and critical thinking. Is able to successfully complete all roles within the department at any given time. Compliance and Program Development: 1. Collaborates with Care Management Leadership in order to successfully implement new policies and procedures. 2. Oversees departmental compliance by ensuring that the team adheres to established policies and procedures. 3. Ensures that the Care Management systems and tools are being utilized as designed including staying up to date with system updates and upgrades. 4. Monitors quality and productivity standards in order to manage inidual performance as well as the team's overall performance. Travel: Less than 10% of the time may be required. Work Type: Hybrid employee - splits time between working remotely and working in the office.

Minimum Qualifications: Education - If a RN, bachelor's degree required. Master's degree preferred. Must have a valid, active unencumbered Nursing license or temporary permit approved by the Georgia Licensing Board. Experience - 7 years minimum experience with at least 5 years in a management position Licensure - LMSW/LCSW will be accepted in lieu of RN requirements. ACM or CCM certification preferred within a year of hire or eligibility Certification - 3 years of experience in Case Management (CM) required. 3 years healthcare experience required. Knowledge, skills, and ability requirements: - Leadership experience preferred. Proven ability to coach, mentor, and lead. - Demonstrates leadership abilities.

Additional Details

Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.

Emory Healthcare is committed to providing reasonable accommodations to qualified iniduals with disabilities upon request. Please contact Emory Healthcare’s Human Resources at [email protected]. Please note that one week's advance notice is preferred.

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Occupational Health Nurse

Columbus, OH

On-site (min. 4 days a week, 1 day remote)

(on-call coverage after standard work hours will be required)

The Occupational Health Nurse Supports the business to reach its objectives by using occupational health and wellbeing expertise to ensure compliance with all applicable regulatory federal and state guidance. Mitigates current and future occupational health risks and business costs through business partnerships. Empowers Associates with the necessary tools to achieve and maintain a lifestyle of health, through proactive interventions and serving as a trusted resource.

What are we looking for?

• Minimum 3+ years Occupational Health experience

• BS in Nursing required, Master's preferred

• Registered Nurse License required

• Current CPR certification

• Ability to work independently and autonomously

• Project management experience a plus

• Previous stakeholder management experience

• Strong Business Acumen required

• Must have strong collaboration, critical thinking and influencing skills

• Workers' Compensation experience preferred

• Ability to travel 10-15% to sites supported is required

Nice to have

• COHN/S (Certified Occupational Health Nurse) preferred

• CAOHC Hearing Conservation Certification preferred

• Previous experience working in a manufacturing site/ in a dynamic fast-paced environment

What would be your key responsibilities?

• Build trusted, credible partnerships with site leaders and stakeholders (HSE, Facilities) to drive healthy culture change through influence.

• Collaborate with other members of the Associate Health & Wellbeing team to deploy strategy, amplify impact, identify synergies for health promotion, and inspire healthy habits.

• COE level expertise to support site initiatives and escalations on health and well-being related issues

• Translation of population-health data, clinical dashboards, and insights to create customized reports that identify gaps, validate program investments, evaluate program effectiveness, and monitor outcomes against targets.

• Actively participates in communities of practice to share learnings, tools, practices, experiences and to support team.

• Proactively seeks continuous learning opportunities and leverages technology to advance the practice of Occupational Health within Mars.

• Develop and implement an action plan for addressing the key health risks for the site based on all applicable data sources. Developing the plan requires awareness and analysis of site population health data. Implementation requires excellent communication and organizational skills, and ability to manage health promotion activities.

• Maintains and safeguards confidentiality of employee health information and health records as mandated by HIPPA and Mars Inc Policy. The role requires current knowledge of a changing regulatory environment including OSHA regulations and Mars Inc requirements, US and state labor laws and any other country laws and regulations.

• Provides health care education designed to prevent injury and illness by promoting effective management of occupational and non-occupational health issues.

• Supports benefit utilization through health fairs and partnership with the Benefits organization

• Regularly interacts with all Associates as part of regular walk throughs, inspections, risk assessments, and/or self-audits.

• Provides clinical nursing assessment, nursing diagnosis and management of occupational injuries and illnesses, following current Nursing Guidelines and Medical Directives.

• Management of country, OSHA, and Mars Inc regulated health monitoring programs including hearing conservation, respirator use, bloodborne pathogens, sensitizers, and others as determined by site assessment tools. This may include related worker training, hazard communication and detailed awareness of occupational hygiene characterization of the work environment.

• Identifies Associates with actual or potential occupational exposures, including chemical, biological, and ergonomic, and determines the need for baseline and annual medical surveillance.

• Ensures that all regulatory processes for work-related injury/ illness claims are followed while maintaining a strong partnership with adjusters, site leadership and risk management.

• Liaises with HSE staff by identifying trends in Occupational Injuries/Illnesses and supporting the resolution of unsafe conditions at the site, assisting with incident investigation as needed and supporting safety initiatives within the workplace.

• Participate in workplace ergonomic assessments for both supply and non-supply safety

• The job holder requires substantial influencing skills to be successful. It will be necessary to influence health and safety behavior and decision making at the site level to drive and support a culture of health and well-being.

What can you expect from Mars?

• Work with over 130,000 with erse and talented Associates, all guided by The Five Principles.

• Join a purpose driven company, where we're striving to build the world we want tomorrow, today.

• Best-in-class learning and development support from day one, including access to our in-house Mars University.

• An industry competitive salary and benefits package, including company bonus.

Mars does not sponsor visas for this role.

This position is not eligible for relocation benefits.

#LI-onsite

#LI-MS1

Title: Senior Quality Engineer - Global Post Market Support

Location: Arden Hills, MN, US, 55112

Additional Location(s): US-MN-Arden Hills; US-MA-Marlborough; US-MN-Maple Grove

Hybrid

Job Description:

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of erse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.           

About the role:

Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work.

This global role is responsible for developing and maintaining standardized complaint handling processes for post-market support teams across all Boston Scientific isions. You will partner with global and isional stakeholders to drive regulatory compliance, operational excellence and continuous improvement across complaint handling systems and processes.

Work model, sponsorship:

At Boston Scientific, we value collaboration and synergy. This is a hybrid position (in office minimum three days per week) with the flexibility to be located in Arden Hills, MN, Maple Grove, MN or Marlborough, MA. You will have the opportunity to discuss your preferred working location with your Talent Acquisition Specialist. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. 

Your responsibilities will include:

• Collaborate with isional and global teams on complaint handling projects and corrective and preventive actions (CAPAs).
• Support regulatory compliance through effective training, documentation and audit readiness activities.
• Evaluate the adequacy and compliance of systems, operations and practices against regulatory requirements and internal procedures; serve as a subject matter expert during internal and external audits.
• Coordinate with global and isional teams to develop and maintain clear documentation, including standard operating procedures (SOPs), work instructions and control plans to ensure consistency and compliance.
• Provide technical leadership to a network of global and isional subject matter experts responsible for monitoring complaint handling processes.
• Partner cross-functionally with complaint handling, risk management and IT/systems teams to ensure alignment and effectiveness.
• Lead and support root cause investigations for recurring process failures and implement effective CAPAs.
• Drive continuous improvement initiatives using quality engineering principles and critical thinking, ensuring alignment with regulatory requirements.
• Define and establish process requirements based on customer needs, translating process outputs into actionable insights for downstream stakeholders.

Required qualifications:

• Minimum of a bachelor’s degree.
• Minimum of 5 years' experience in quality within the medical device or pharmaceutical industry.
• Strong understanding of post-market regulatory requirements.

Preferred qualifications:

• Demonstrated problem-solving, influencing and critical thinking skills.
• Experience with project management methodologies and tools.
• Experience working in a global or multi-isional environment.
• Experience with statistical process control (SPC) and other statistical tools for quality data analysis, including application to business processes.
• ASQ Certified Quality Engineer (CQE), Lean Six Sigma or similar certification.
• Working knowledge of medical device regulations, including EU MDR, ISO 13485 and ISO 14971.

Requisition ID: 627626 

Minimum Salary: $ 85000 

Maximum Salary: $ 161500 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an inidual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

Title: Hybrid Remote BCBA

remote type Hybrid

locations Lincoln, CA - 95648

time type Full time

Job Description:

Clinicians With Purpose and Impact

Advancing Quality Care and Clinical Excellence

BCBAs at CSD

Board Certified Behavior Analyst (BCBA) ready to join a breakthrough and innovative ABA program focused on clinical quality and client experience. This position combines clinical expertise, strategic oversight, and team mentorship to ensure high-quality, ethical ABA services.

Starting Pay: $85,000-$95,000 annually, based on experience

About the Opportunity

As a BCBA, you will:

• Oversee and ensure fidelity of ABA programs
• Support and coach Clinical Leaders (Mid-Level Supervisors) and Behavior Specialists
• Complete and review treatment plans, progress reports, and documentation
• Ensure compliance with clinical and payer standards
• Lead trainings and clinical development initiatives
• Partner with Regional Directors and Operations teams on initiatives, quality, compliance, and more

What Excellence Looks Like

• High-quality, data-driven clinical programs
• Strong, supported clinical teams
• Families who trust the care provided

Benefits, Growth & Clinical Support

• Competitive salaried compensation
• In-house CEUs and annual CEU allowance for conferences and external learning
• Opportunities to participate in clinical research initiatives
• Senior clinical support and collaboration with Regional and Executive Clinical Leadership
• Dedicated administrative and operational support, allowing focus on clinical quality
• Leadership development opportunities within a growing organization

About You

This role is ideal for a BCBA who:

• Brings strong clinical judgment and experience overseeing ABA programs
• Is enthusiastic about exploring innovative ABA programs
• Enjoys mentoring and developing Clinical Leaders (Mid-Level Supervisors) and clinicians
• Values high standards, ethical practice, and data-driven decision-making
• Is comfortable leading teams while navigating clinical and operational complexity
• Wants to influence clinical excellence at both the inidual and systems level

Requirements

• Master's degree in a related discipline
• Active BCBA credential
• Minimum two years of professional ABA experience
• Strong communication and clinical leadership skills
• Ability to travel within service areas

Ready to Apply?

If you've been looking for a role where your work matters, where kids look forward to seeing you, and where your career path is clear - this is it.

Join us. Let's light up lives together.

CSD is a proud equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

In accordance with the Fair Chance Act, we will consider for employment qualified applicants with arrest and conviction records. CSD is dedicated to ensuring fair hiring practices and encourages all iniduals, including those with prior criminal histories, to apply.

#LI-Hybrid

About Us

At Center for Social Dynamics (CSD), we believe that every child deserves a chance to shine. We're a passionate team on a mission to open up a world of possibilities for iniduals with autism and other developmental needs-through science, compassion, and a whole lot of heart.

From our very first session to each milestone we celebrate, we bring the power of play, connection, and evidence-based care to every moment. With services that are as unique as the iniduals we support, we meet kids where they are-at home, in schools, and in communities-and guide them on a path toward growth.

We live our TRUE values-Transparency, Respect, Understanding, and Excellence-in everything we do. As a fast-growing leader in the field, we're known for our vibrant culture, hands-on training, and career pathways that help you grow just as much as those we serve.

At CSD, we don't just change lives-we light them up.

About Our Values

• Transparency in the work that we do and the actions we take to achieve our mission. There are no hidden agendas or motives at Center for Social Dynamics. Each family's unique cultures, values, and generational dynamics.

• Understanding through tolerance, cooperation, and empathy in the pursuit of our mission. We never lose sight of who we are, the people we serve, and our purpose and meaning.

• Respect for all and the value that everyone brings towards accomplishing our mission. No one at CSD is worth more or less, and together we are greater than the sum of our parts.

• Excellence in our drive, passion, and commitment to our mission. CSD will always do what it takes to deliver the best, leave no one behind, and champion our cause.

CSD is a proud equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Physical requirements may include but is not limited to:

• Constant visual stimulation, including close vision, distance vision, reading, computer work

• Constant sitting; frequent up and down out of chair

• Constant use of telephone, speaking, listening

• Constant document handling, use of copier and fax machine, filing

• Frequent typing, use of computer

• Occasional walking around building

• Occasional bending, reaching, stooping, pulling

• Occasional lifting, carrying, moving of items up to 20 pounds

• Occasional walking to, bending to enter, sitting and using upper and lower limbs to drive car

Title: Pharmacy Administration Coordinator

Location: Administrative Office - Tigard, OR 97223

Salary Range $22.33 - $29.05

Level Entry

Position Type Full Time

Job Shift Day

Education Level High School Diploma or Equivalent

Category Nonprofit - Social Services

Job Description:

Who We Are:

Neighborhood Health Center is a non-profit organization local to Portland, OR serving underserved patients in the areas of primary care, internal medicine, dental services and more. Our patient-centered approach to care honors the unique needs and circumstances of each inidual patient. NHC sees people, not problems, and recognizes that the time spent as a patient in a doctors office is only one factor in a persons overall health. Our leading edge, integrated clinical teams work in partnership with patients, their families, and the communities we serve to provide whole-person care, prevention, and ongoing support.

NHC is an Equal Opportunity Employer. We celebrate differences in the workplace and do not discriminate in employment opportunities or practices on the basis of race, color, religion, gender (sex), national origin, age, veteran status, sexual orientation, gender identity, disability, genetic information or any other characteristic protected by law.

Why work with us?

• We are a non-profit organization, passionate about providing the underserved population with medical and dental services across the greater Portland area, committed to making a difference daily.
• We offer our employees a competitive compensation and benefits package which includes 20 days of PTO (based on full time employment), 9 paid holidays, health/dental/vision insurance, quarterly wellness reimbursements, generous 401k retirement plan with employer match, employer paid disability insurance, EAP and life insurance.
• Our employees voted NHC a Top Workplace in 2020, 2021, 2022, 2023, 2024 and 2025!

Job Title: Pharmacy Administration Coordinator

Department: Pharmacy

Reports To: 340B Pharmacy Manager

Work Type: Hybrid

Classification: Non-Exempt

Language Differential: Ineligible

SUMMARY

The Pharmacy Administration Coordinator provides primary administrative support for pharmacy prior authorization workflows, ensuring timely processing, accurate documentation, and effective communication with pharmacies, patients, and insurance payors. The role focuses heavily on managing high volume prior authorization requests, tracking cases, and supporting approval rate goals while preventing backlogs.

Additionally, the coordinator supports the 320B Pharmacy Manager with reporting, compliance, inventory, and audit-readiness tasks. This position requires strong attention to detail, healthcare administrative experience, and the ability to manage competing priorities in a fast-paced environment.

Essential Job Duties

Prior Authorization Support (80%)

The coordinator will serve as the primary administrative resource for all prior authorization workflows, including:

• Index all incoming pharmacy faxes in OnBase and route documents to the PA In-Basket accurately and in a timely manner.
• Triage PA In-Basket items to distinguish new authorization requests from duplicate submissions.
• Close completed or duplicate requests and create electronic encounters for new PA cases.
• Support outbound communication with pharmacies, patients, and insurance payers regarding PA approvals, denials, and follow-up requirements.
• Follow up with insurance carriers within 2 business days for urgent PA requests and within 5 business days for routine medication requests.
• Provide coverage during PTO, leave, and high-volume periods to prevent backlog accumulation.
• Assist in maintaining pending PA case counts.
• Support documentation and tracking efforts to sustain a PA approval rate of 64% or higher.

340B Program Support (20%)

The coordinator will support the 340B Pharmacy Manager with recurring administrative and compliance tasks, including:

• Run and organize monthly Walgreens and Wellpartner reports for 340B tracking and reconciliation.
• Prepare contract pharmacy claims files for submission to 340B ESP in accordance with program deadlines.
• Generate monthly purchasing and inventory reports to support program accuracy and audit readiness.
• Support purchase order (PO) creation for clinic locations based on PAR level requirements.
• Assist with medication recalls, E-kit restocking, and routine inventory checks.
• Maintain audit-ready documentation at all times in compliance with 340B program requirements.
• Complete all monthly reports by deadlines set by the 340B Pharmacy Manager.

Qualifications

Education and/or Experience

Required

• High school diploma or equivalent; associate degree preferred.
• Minimum 1–2 years of healthcare administrative experience, preferably in a pharmacy, clinical, or insurance-related setting.
• Demonstrated experience with Epic.
• Strong attention to detail and accuracy when processing high volumes of transactions
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Effective written and verbal communication skills for patient and provider-facing correspondence.
• Ability to manage competing priorities and maintain performance under volume pressure.