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Clinical Research Project Manager Jobs in Reston, VA

Research Project Manager

College Park, MD ยท On-site

$140K - $165K/yr

Research Project Manager TAP Engineering | College Park, MD | Full Time Clearance Required: Active TS/SCI with Polygraph | Experience: 7+ Years | Compensation: $140,000 - $165,000 Position ...

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Research Project Manager

College Park, MD ยท On-site

$125K - $140K/yr

Research Project Manager TAP Engineering | College Park, MD | Full Time Clearance Required: Must be eligible to obtain a TS/SCI with Polygraph | Experience: 7+ Years | Compensation: $125,000 - $140 ...

Apply Early

Clinical Research Manager

Bethesda, MD ยท On-site

$105K - $120K/yr

About the Position The Clinical Research Manager oversees on-site research operations to include ... About the Project This RION study is within the MIRROR portfolio. This is a Phase 1b, open-label ...

Clinical Research Manager

Bethesda, MD ยท On-site

$105K - $120K/yr

About the Position The Clinical Research Manager oversees on-site research operations to include ... About the Project This RION study is within the MIRROR portfolio. This is a Phase 1b, open-label ...

Clinical Study Manager, Lead CRA, Project Manager, etc.) independently schedules and conducts ... Expertise in clinical research operations, including interpretation and implementation of country ...

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Showing results 1-20

Clinical Research Project Manager information

See Reston, VA salary details

$52K

$89.5K

$137.3K

How much do clinical research project manager jobs pay per year?

As of Jul 5, 2026, the average yearly pay for clinical research project manager in Reston, VA is $89,503.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,400.00 and $95,200.00 per year, depending on experience, location, and employer.

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

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What does a Clinical Research Project Manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are some common challenges faced by Clinical Research Project Managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What are the key skills and qualifications needed to thrive as a Clinical Research Project Manager, and why are they important?

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.
What are the most commonly searched types of Clinical Research Project jobs in Reston, VA? The most popular types of Clinical Research Project jobs in Reston, VA are:
What are popular job titles related to Clinical Research Project Manager jobs in Reston, VA? For Clinical Research Project Manager jobs in Reston, VA, the most frequently searched job titles are:
What cities near Reston, VA are hiring for Clinical Research Project Manager jobs? Cities near Reston, VA with the most Clinical Research Project Manager job openings:

$79K - $101K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 6 days ago


Job description

Mid-Atlantic Permanente Medical Group (MAPMG) invites applications for a Research Project Manager to join our Mid-Atlantic Permanente Research Institute (MAPRI) department. This position is a full-time opportunity based out of our regional office located in Washington, D.C. with a hybrid work model.

Mid-Atlantic Permanente Medical Group is comprised of more than 1,700 Permanente physicians and nearly 300 staff professionals who come together to make a positive impact on the health and lives of more than 800,000 members in Virginia, Maryland, and the District of Columbia.ย 

Reporting to the Senior Director, MAPRI, the Research Project Manager coordinates highly visible, sensitive, and multifaceted healthcare research projects in accordance with established protocols, budgets, timelines, and regulatory requirements. You will oversee post-award project activities, monitor progress and compliance, coordinate research teams, and help ensure projects involving patient data are completed on time, within budget, and in accordance with Health Insurance Portability and Accountability Act (HIPAA) and Institutional Review Board (IRB) requirements.ย 

You can expect to:

  • ย Develop and implement tracking systems to monitor study timelines, goals, budgets, deliverables, and project progress.
  • ย Coordinate post-award research activities, including task planning, responsibility assignments, deadlines, participant tracking, and data quality monitoring.
  • ย Partner with principal investigators, research staff, clinical teams, managers, and regional stakeholders to support protocol implementation and resolve study-related issues.
  • ย Provide timely project status reports and updates to investigators, senior management, and other stakeholders.
  • ย Monitor research activities for compliance with study protocols, IRB requirements, federal regulations, internal policies, and HIPAA standards.
  • ย Support IRB applications, continuing reviews, protocol clarification, budget monitoring, and the reporting of compliance concerns.
  • ย Coordinate manuscript development and track research publications, presentations, and participation in national and international conferences.
  • Identify project risks, timeline delays, protocol deviations, and operational challenges, and implement appropriate solutions in collaboration with investigators and senior project managers.

What is required:

  • Bachelorโ€™s degree in Public Health, Healthcare Administration, or a related field with at least four years of research project management experience, or a masterโ€™s degree in a related field with at least two years of relevant experience.
  • Experience coordinating healthcare research projects involving protocols, budgets, timelines, deliverables, and regulatory requirements.
  • Experience supporting Institutional Review Board applications, continuing reviews, and compliance with human subjects research requirements.
  • Experience managing projects involving patient data and maintaining compliance with HIPAA and applicable data-use requirements.
  • Proficiency with Tableau, Microsoft Word, Excel, PowerPoint, and Access.
  • Experience with REDCap, qualitative analysis software such as NVivo or Atlas.ti, and project management tools such as Microsoft Project or Smartsheet preferred.
  • Strong organizational, analytical, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Strong interpersonal, leadership, and stakeholder management skills.
  • Must be able to commute to Washington, D.C. on an as-needed basis.
  • Candidates must either currently live in or be willing to relocate to the Washington D.C. metropolitan area.
  • Must provide documentation for the influenza vaccine as a condition of employment.

Competitive Benefits:

  • Competitive compensation package
  • 100% employer-funded medical and dental insurance premiums for employees and families effective on the first day of employment
  • Generous paid time off, including vacation, holidays, and sick leave, plus maternity and parental leave
  • Pension plan, and 401(k) retirement plan with employer contributions
  • Life insurance, short-term disability, and long-term disability coverage
  • Education reimbursement

The starting annual salary for this position is 85,000. The salary takes into account an applicantโ€™s skills and qualifications, certain degrees and certifications, prior job experience, training, market data, and other relevant factors. In addition to the salary above, MAPMG offers rich benefits that add substantial value to the total compensation package.

MAPMG continuously works to identify and mitigate healthcare inequities and strives to provide an inclusive, supportive environment for physicians and staff. We encourage applicants of any race, color, religion, sex, sexual orientation, gender identity, or national origin who value diversity and are committed to practicing culturally competent healthcare.

External hires must pass a background check and drug screening.