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Clinical Research Program Manager information

See Renton, WA salary details

$50.1K

$104.2K

$168.2K

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

As of Jun 22, 2026, the average yearly pay for clinical research program manager in Renton, WA is $104,163.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $118,100.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by Clinical Research Program Managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What does a Clinical Research Program Manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

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

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

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

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.
What job categories do people searching Clinical Research Program Manager jobs in Renton, WA look for? The top searched job categories for Clinical Research Program Manager jobs in Renton, WA are:
What cities near Renton, WA are hiring for Clinical Research Program Manager jobs? Cities near Renton, WA with the most Clinical Research Program Manager job openings:
Clinical Research Program Manager jobs near you
Clinical Research Coordinator I/II

Clinical Research Coordinator I/II

Benaroya Research Institute

Seattle, WA

$30 - $44.69/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

Join a collaborative team at the Clinical Trials Unit of Benaroya Research Institute (BRI), where your work will directly support cutting-edge clinical research in partnership with Virginia Mason physicians. Our studies focus on a variety of specialties including Cardiology (treatment of either new medications or cardiac devices), Neurology, and Allergy studies.
This role offers exposure to a wide range of clinical trials across various phases of development. You will be part of a supportive, team-oriented environment with unparalleled support from our physicians, clinic staff, and dedicated study teams. We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to support our Principal Investigators in executing high-quality research protocols.
Schedule: Typically Monday through Friday from 8:00 AM to 4:30 PM, with a 30-minute lunch break. Work schedule may vary.


  • Facilitate clinical research, including collaboration with affiliate or partnering research sites and conducting BRI-based studies
  • Prepare for new studies, including regulatory document filing and study monitor visit preparation
  • Screen and recruit study subjects, obtain informed consent, and document subject history
  • Review adverse events, concomitant medications, and ensure protocol compliance and subject safety
  • Handle test articles (TA), complete case report forms, and maintain source documents
  • Manage proper standard or research billing and ensure site quality
  • Coordinate subject care, including appointment scheduling, record reviews, treatment coordination, and health assessments
  • Collect vital signs, perform telephone triage/screening, and assist with subject arrivals
  • Conduct phlebotomy, specimen processing using universal precautions, and other procedures as appropriate
  • Participate in process improvement activities and develop corrective and preventive action plans

  • Clinical Research Coordinator I

    • Minimum of one year full-time related experience required
    • Must maintain subject and document confidentiality at all times
    • Understand and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, IRB, and institutional policies and procedures
    • Requires good medical knowledge, including medical terminology and basic subject care
    • May require phlebotomy and vital sign collection skills, as well as the ability to operate centrifuges and EKG machines
    • Preferred: Higher education or vocational training specializing in healthcare
    • May require healthcare licensure or other specialized training

    Clinical Research Coordinator II

    • Minimum of two years full-time related experience in clinical research required
    • Must maintain subject and document confidentiality at all times and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, Institutional Review Boards (IRB), and institutional policies and procedures
    • Ability to provide guidance or informal supervision to a Research Assistant or CRC I in the conduct of their study, as applicable
    • Bachelor’s degree and SOCRA or ACRP certification strongly preferred
    • A Master’s degree in clinical research or a related field, or an M.D., may substitute for the two years of clinical research experience

  • Clinical Research Coordinator I - $25.66 to $37.21 hourly
  • Clinical Research Coordinator II - $30.00 to $44.69 hourly

  • Medical, dental, vision insurance
  • Flexible spending accounts: health care, dependent care, commuter
  • Short and long-term disability
  • Life and AD&D insurance
  • 403(b) retirement plan with matching funds after one year of employment
  • PTO: 13 holidays, three weeks of vacation and two weeks of sick leave per year
  • Employee assistance program
  • Educational assistance program
  • Subsidized ORCA pass
  • Wellness benefits
  • Voluntary benefits

The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities to patients, giving them access to clinical trials for over 100 different conditions including cancer, digestive disease, cardiology, and neuroscience. The Clinical Research Program at BRI oversees all clinical research at Virginia Mason Medical Center, combining the expertise of a world-renowned research institute with remarkable healthcare to support studies that contribute to improving the diagnosis, treatment, and prevention of a variety of diseases.

BRI is an independent, nonprofit research institute affiliated with Virginia Mason Franciscan Health and based in Seattle. Our culture is based on the values of collaboration, respect, innovation, and inquiry; team members work together to support patients and clinicians with the goal of better outcomes for all.

At BRI, each role is valued and an important contributor to our vision and mission. BRI is committed to a safe, caring and diverse workplace; as well as to taking action to further our commitments to foster inclusion, equity and belonging so employees feel comfortable bringing their full selves to work. Consider making a difference by joining our team. Because together, we are powering possibility.
To learn more, visit benaroyaresearch.org and connect with us on Facebook, Instagram, Threads,  LinkedIn, Bluesky and YouTube.
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. If you need an accommodation or assistance completing the online application, please contact Human Resources at 206-342-6547 or email jobs@benaroyaresearch.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.


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