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Medical Device Clinical Expert Jobs (NOW HIRING)

RQMIS Inc

Clinical Trials Project Manager

Amesbury, MA · On-site

RQMIS Inc. is a fast growing, medical device/biotechnology consultancy with a focus on regulatory strategy/submissions, clinical study design/management and quality systems design/compliance/auditing.

Noctrix Health

Director, Clinical Affairs

Pleasanton, CA · On-site

$89K - $121K/yr

Our team of medical device specialists, neuroscientists, and consumer electronics engineers is ... The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ...

Noctrix Health

Director, Clinical Affairs

Pleasanton, CA · On-site

$89K - $121K/yr

Our team of medical device specialists, neuroscientists, and consumer electronics engineers is ... The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ...

Intelas

Medical Device Integration Coordinator

Chicago, IL · On-site

$75K - $80K/yr

Intelas, a Compass Healthcare company, delivers smarter asset management by blending expert service ... Our programs support 100% regulatory compliance and drives 98% equipment uptime--so clinicians can ...

Heart Medical, LLC

Be Seen First

Medical Device Sales Representative

Atlanta, GA · On-site

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Medical Device Sales Representative Territory: Southeastern states Employment Type: Full-Time ... Collaborate with marketing, clinical, and operations teams to support product launches and growth ...

Edwards Lifesciences Corporation

Expert knowledge of the FDA's Quality System Regulations; experience working within a Quality ... medical records and clinical data to assess adverse events and potential device-related risks

Edwards Lifesciences Corporation

Expert knowledge of the FDA's Quality System Regulations; experience working within a Quality ... medical records and clinical data to assess adverse events and potential device-related risks

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Medical Device Clinical Expert information

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How much do medical device clinical expert jobs pay per year?

As of Sep 13, 2026, the average yearly pay for medical device clinical expert in the United States is $112,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,000.00 and $119,000.00 per year, depending on experience, location, and employer.

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For Medical Device Clinical Expert jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Clinical Expert job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $112,500 per year, or $54.1 per hour.

Clinical Trials Project Manager

Amesbury, MA • On-site

RQMIS Inc
Business Management Consulting • 1 - 10 employees
Learn more about RQMIS Incexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 27 days ago

Job description

RQMIS Inc. is a fast growing, medical device/biotechnology consultancy with a focus on regulatory strategy/submissions, clinical study design/management and quality systems design/compliance/auditing.

OVERALL RESPONSIBILITIES:

The Clinical Trials Project Manager will:

  • Develop/implement/ manage all aspects of clinical trials in domestic and international countries for our clients.
  • Provide training to clients and internal staff on such areas as clinical trial management, good clinical practices (GCPs), FDA Biomonitoring, CRF design, clinical report writing, Clinical Study Monitoring, etc.

POSITION DUTIES & RESPONSIBILITIES:

  • Manage all aspects of clinical projects
  • Provide training to clients and internal staff
  • Write departmental procedures and assist in training efforts
  • Participate in special projects as needed
  • Travel required (up to 30 to 50%)
  • Other duties as assigned

EDUCATION & PROFESSIONAL EXPERIENCE:

  • Bachelor’s degree in clinical/science field, or similar work experience
  • 5 to 7 years experience in medical device clinical trials
  • Previous supervisory or team leadership experience
  • Knowledge of domestic/international medical device regulations
  • Strong attention to detail
  • Strong computer skills, including word processing, spreadsheet and data programs
  • Good oral and written communication skills
  • Good leadership skills
  • Ability to manage several tasks simultaneously while continuously assessing company and/or departmental priorities

Company Description

RQMIS Inc is located north of Boston Massachusetts area is a fast growing medical device/ biotechnology consultancy with focused in three principle areas, regulatory strategy/submissions, clinical study design/management and quality systems design/compliance. RQMIS Inc has been providing companies with strategic guidance on how to effectively navigate the FDA, UK and EU regulations for over 25 years in around the world.