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Clinical Research Project Manager Jobs in Bothell, WA

This position is responsible for implementing multiple research projects in human subjects. About this Opportunity This position reports to the Clinical Research Manager and will utilize operational ...

Reporting to the Principal Investigator the Research Coordinator will be responsible for actively managing and conducting several funded human subject clinical projects and industry-sponsored ...

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Clinical Research Project Manager information

See Bothell, WA salary details

$55.9K

$96.2K

$147.6K

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

As of Jun 21, 2026, the average yearly pay for clinical research project manager in Bothell, WA is $96,174.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,900.00 and $102,300.00 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 popular job titles related to Clinical Research Project Manager jobs in Bothell, WA? For Clinical Research Project Manager jobs in Bothell, WA, the most frequently searched job titles are:
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What cities near Bothell, WA are hiring for Clinical Research Project Manager jobs? Cities near Bothell, WA with the most Clinical Research Project Manager job openings:

Clinical Research Project Manager II

Fred Hutchinson Cancer Research Center

Seattle, WA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

Overview

Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.

With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world's leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world's deadliest diseases and make life beyond cancer a reality.

At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.

The Clinical Research Project Manager will lead a diverse portfolio of projects to enhance operational efficiencies in the administration and management of the Fred Hutch and Cancer Consortium clinical trials. The Project Manager reports into the central clinical trials office, Clinical Research Support, and manages internal and external collaborations across multiple teams and departments and drives decisions to ensure project milestones and deliverables are met in an efficient manner. This role will be responsible for self-directing large, complex projects from initiation to completion. The role will be responsible for defining project scope, resources, and stakeholders, identifying technical solutions, and will work closely with CRS leadership to develop project deliverables that may include standard operating procedures (SOPs), tools, workflows, and process maps. This position requires flexibility in a dynamic environment to ensure the prioritization of projects is aligned with departmental and institutional strategic goals.

At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.

This role will have the opportunity to work partially at our campus and remotely, and will need to be present on-campus as needed for projects.

Responsibilities
  • Lead projects of varying complexity and size to support operational efficiencies across the Fred Hutch and Cancer Consortium clinical research enterprise.
  • Scope projects, defining resources, stakeholders, and potential barriers with risk mitigation strategies.
  • Convene cross-functional stakeholder meetings, tracking action items and key decisions to maintain progress.
  • Establish, monitor, and communicate project plan and timelines, ensuring milestones are met.
  • Manage internal and external stakeholders, fostering effective communication and collaboration.
  • Develop, implement, and manage standard tools and processes to manage project requests and work closely with CRS leadership to maintain and vet prioritized project list, adjusting as appropriate.
  • Provide document management and version control of all project-related materials.
  • Stay abreast of relevant technical solutions to support project coordination and operational solutions.
  • Develop and maintain relationships with internal and external stakeholders, representing the project to other departments, funding sources, affiliated individuals or institutions, and outside organizations.
  • Facilitates task management and tracking both during and outside of meetings. Manages expectations, sets appropriate deadlines and ensures the timely completion of work.
  • Create, update, and manage project deliverables including standard operating procedures (SOPs), process maps, templates, and guidance documents in support of implementation and change management of new system or processes.
  • In partnership with departmental leadership, understand areas of cross-functional points of intersection and opportunities for improved integrations.
  • Critically review processes, workflows, and SOPs for consistency, high-level operational, and institutional considerations.
  • Perform other duties as assigned to support the team and organizational goals.
Qualifications

MINIMUM QUALIFICATIONS:

  • BA/BS in related field or equivalent experience.
  • Minimum of four years project/study management experience with a master's degree or six years' experience with a bachelor's degree, in a research setting.
  • Excellent written and verbal communication skills.
  • Strong supervisory skills and budgeting experience.
  • Grant and contract experience.

PREFERRED QUALIFICATIONS:

  • MA/MS desired.
  • Oncology clinical research experience in an academic setting.
  • Clinical study coordinator or other clinical research management experience.
  • Research systems workflow experience.
  • Demonstrated ability to successfully self-direct projects from initiation to completion.
  • Demonstrated excellent human relations, facilitation and influencing skills to deal effectively with all levels of employees and management.
  • Ability to effectively create and execute project steps toward desired end results.
  • Ability to quickly synthesize complex issues to move project forward.
  • Knowledge of clinical protocol development, review and approval process.
  • Familiarity with applicable federal regulations and guidelines pertaining to clinical research, including IND applications.
  • Proven ability to communicate effectively verbally and in writing.
  • Excellent writing and editing skills.

The annual base salary range for this position is from $88,712 to $133,058, and pay offered will be based on experience and qualifications.

This position may be eligible for a sign-on bonus.

This role will have the opportunity to work partially at our campus and remotely, and will need to be present on-campus as needed for projects.

Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).

Additional InformationWe are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.Employment Type: FULL_TIME