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RQMIS Inc

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Clinical Trials Project Manager

Amesbury, MA · On-site

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 ...

University of Rochester

$70K - $105K/yr

Mentors, trains, and manages more junior staff as part of a study project team. Provides professional direction within clinical trials coordination team. Oversees study team interactions with study ...

Worldwide Clinical Trials

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide Worldwide Clinical Trials Project ...

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How much do clinical trials project manager jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for clinical trials 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.

What does a clinical trials project manager do?

A Clinical Trials Project Manager oversees the planning, execution, and completion of clinical research studies. They coordinate teams, manage timelines and budgets, ensure regulatory compliance, and communicate with stakeholders such as sponsors and regulatory agencies. Their role is crucial in ensuring that clinical trials run smoothly, meet all quality standards, and produce reliable data for new medical treatments or drugs.

What are the key skills and qualifications needed to thrive as a clinical trials project manager, and why are they important?

To thrive as a Clinical Trials Project Manager, you need a strong background in life sciences, clinical research experience, and often a relevant degree or certification such as a PMP or ACRP credential. Familiarity with clinical trial management systems (CTMS), regulatory compliance standards like GCP, and project management tools is essential. Excellent organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These skills ensure trials are conducted efficiently, compliantly, and safely, supporting successful study outcomes.

What are the most common challenges faced by clinical trials project managers and how can they be addressed?

Clinical Trials Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance across multiple sites, and coordinating communication among diverse stakeholders. To address these, it is important to establish clear project plans, foster open communication channels with site teams and sponsors, and stay updated on regulatory requirements. Utilizing project management tools and regularly scheduled meetings can also help ensure that tasks are on track and potential issues are identified early.

What is the difference between Clinical Trials Project Manager vs Clinical Research Coordinator?

AspectClinical Trials Project ManagerClinical Research Coordinator
CredentialsBachelor's degree, often with project management certificationBachelor's degree in health sciences or related field
Work EnvironmentOversees multiple trials, manages teams, and coordinates with sponsorsHandles daily trial activities at clinical sites, interacts directly with participants
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical sites
Search & Comparison IntentFocuses on project management in clinical trialsFocuses on site-level trial coordination

The Clinical Trials Project Manager primarily oversees multiple clinical trials, managing teams and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at clinical sites, working directly with participants. Both roles require relevant healthcare or research credentials but differ in scope and responsibilities within the clinical research process.

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Clinical Trials Project Manager jobs near you
Infographic showing various Clinical Trials Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% 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
Learn more about RQMIS Incexternal

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.