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Medical Device Clinical Project Manager Jobs (NOW HIRING)

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RQMIS Inc. is a fast growing, medical device/biotechnology consultancy with a focus on regulatory ... The Clinical Trials Project Manager will: * Develop/implement/ manage all aspects of clinical ...

Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract research ...

Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $70.00 - $79.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm Overview Join a collaborative, fast-paced ...

Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $70.00 - $79.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm Overview Join a collaborative, fast-paced ...

Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $70.00 - $79.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm Overview Join a collaborative, fast-paced ...

Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $70.00 - $79.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm Overview Join a collaborative, fast-paced ...

Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $70.00 - $79.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm Overview Join a collaborative, fast-paced ...

... medical device technologies are designed to help people live their lives better and healthier ... trial and monitors/manages compliance as part of clinical project management.

Project Manager - Medical Device

Irvine, CA · On-site +1

$81K - $115K/yr

Minimum three (3) years of experience in project management; medical device industry experience, a plus. * Demonstrated knowledge of International Organization for Standardization (ISO) and Food and ...

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How much do medical device clinical project manager jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for medical device clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

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

Infographic showing various Medical Device Clinical Project Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Trials Project Manager

Amesbury, MA • On-site

RQMIS Inc
Business Management Consulting • 1 - 10 employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

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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.