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Decentralized Clinical Trials Project Manager Jobs

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 ...

University of Utah

Serve as the operational administrator for HCI's decentralized clinical trials portfolio ... Design, implement, and manage hub-and-spoke operations that enable decentralized and hybrid ...

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

As of Sep 9, 2026, the average hourly pay for decentralized 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 is a decentralized clinical trials project manager?

Decentralized Clinical Trials (DCT) Project Managers are professionals who oversee the planning, execution, and management of clinical trials that utilize digital tools and remote processes. Unlike traditional clinical trials, DCTs allow participants to contribute data from their homes or local healthcare settings, reducing the need for in-person visits. Project Managers in this field coordinate multiple stakeholders, ensure regulatory compliance, manage timelines, and troubleshoot challenges related to technology and logistics. Their role is crucial in ensuring that decentralized trials run smoothly and deliver reliable results.

What are the key skills and qualifications needed to thrive as a decentralized clinical trials project manager?

To thrive as a Decentralized Clinical Trials Project Manager, you need expertise in clinical research processes, regulatory compliance, and project management, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote patient monitoring tools, and GCP certification is highly valued. Strong communication, problem-solving, and organizational skills help you effectively coordinate teams and manage complex trial logistics. These abilities are crucial for ensuring decentralized trials are executed efficiently, compliant with regulations, and deliver high-quality data.

What are some common challenges faced by a decentralized clinical trials project manager, and how can they be addressed?

A Decentralized Clinical Trials Project Manager often navigates challenges such as coordinating remote study teams, ensuring data integrity from multiple digital sources, and maintaining robust participant engagement. Effective communication and implementing standardized digital platforms can help overcome these hurdles. Additionally, proactive risk management and regular training for team members on new technologies are key to ensuring trial success. Collaboration with IT, regulatory, and clinical teams is crucial to keep decentralized trials running smoothly and compliantly.

What are popular job titles related to Decentralized Clinical Trials Project Manager jobs?

For Decentralized Clinical Trials Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Decentralized Clinical Trials Project Manager job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person 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 23 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.