1

Clinical Trial Risk Based Monitoring Jobs in Seattle, WA

Oncology Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

Hematology Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

Hematology Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

Oncology Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

Strong knowledge of clinical trial databases, CDISC standards, coding dictionaries (e.g., MedDRA ... Familiarity with risk-based quality management principles, GCP requirements, and clinical ...

Director, Clinical Science

Seattle, WA · On-site

$91K - $124K/yr

... Risk Management * Identify opportunities for innovation and improvement in clinical trial ... Consistently monitor for risks and recommend actions to address issues in a timely manner.

... risk management processes. * Monitor evolving health authority guidance and industry standards ... Strong understanding of GCP, clinical trial conduct, drug development processes, and regulatory ...

Head of AI Clinical Excellence

Bothell, WA

$89K - $121K/yr

... risk management processes. * Monitor evolving health authority guidance and industry standards ... Strong understanding of GCP, clinical trial conduct, drug development processes, and regulatory ...

... clinical monitoring activities, enrollment, cycle times, and trial performance indicators. The ... and risk management, adoption, and sustainment. * Champion AI-enabled dashboards and advanced ...

Showing results 21-40

Clinical Trial Risk Based Monitoring information

See Seattle, WA salary details

$19

$45

$79

How much do clinical trial risk based monitoring jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical trial risk based monitoring in Seattle, WA is $45.50, according to ZipRecruiter salary data. Most workers in this role earn between $36.63 and $50.05 per hour, depending on experience, location, and employer.

What is clinical trial risk based monitoring?

Clinical Trial Risk Based Monitoring (RBM) is a strategy used in clinical research to prioritize and focus monitoring activities on the most critical risks to patient safety and data integrity. Instead of monitoring every data point equally, RBM uses data analytics and risk assessment tools to identify which sites, processes, or data require more attention. This approach increases efficiency, reduces costs, and helps ensure that potential issues are detected and addressed promptly. RBM is supported by regulatory agencies and is increasingly adopted in both large and small clinical trials.

How does a clinical trial risk based monitoring professional typically collaborate with cross-functional teams during a study?

In a Clinical Trial Risk Based Monitoring role, you will regularly work with clinical research associates, data managers, statisticians, and regulatory teams to identify and address potential risks throughout a study. Collaboration often involves participating in meetings to review data trends, sharing insights about site performance, and helping to develop mitigation strategies. Effective communication is crucial, as you will be responsible for ensuring that all stakeholders are informed of key risks and recommended actions. This collaborative environment helps drive patient safety, data integrity, and overall trial success.

What are the key skills and qualifications needed to thrive in clinical trial risk based monitoring, and why are they important?

To thrive in Clinical Trial Risk Based Monitoring, you need expertise in clinical research, regulatory compliance, and data analysis, usually supported by a degree in life sciences or related fields. Familiarity with risk assessment tools, EDC (Electronic Data Capture) systems, and GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, critical thinking, and effective communication help professionals proactively identify and address potential risks in trials. These skills are crucial for maintaining data integrity, ensuring patient safety, and optimizing the efficiency and quality of clinical studies.

What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?

AspectClinical Trial Risk Based MonitoringClinical Trial Data Manager
Primary FocusMonitoring trial sites for risks and complianceManaging and ensuring accuracy of trial data
Required SkillsMonitoring protocols, regulatory knowledge, site managementData management, database systems, quality control
Work EnvironmentClinical sites, monitoring visits, remote oversightData centers, clinical trial databases, office setting
CertificationsGCP, monitoring certificationsCDMP, data management certifications

While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.

What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Seattle, WA?

For Clinical Trial Risk Based Monitoring jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Seattle, WA look for?

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Seattle, WA are:

Infographic showing various Clinical Trial Risk Based Monitoring job openings in Seattle, WA as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $94,649 per year, or $45.5 per hour.

$27.50 - $36.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 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 position will work directly with hospital, clinic and research staff in the development, implementation and management of clinical trials.  Responsible for the collection, coordination, processing, and quality control of clinical trial data in accordance with protocols subject to FDA oversight.  Responsible for coordination of long-term follow-up activities associated with these protocols.  Uses judgment in data collection, quality control, liaison, and research coordination activities.  Interacts with patients, physicians, and other clinical providers and support staff within and outside of the Fred Hutch/Seattle Children's UW system including the Fred Hutch Transplant Service.  This individual will work under limited supervision of the Senior Clinical Research Manager and will be required to perform his/her responsibilities with a high level of independence within the scope of study protocol(s) and institutional policies and guidelines.

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.

Responsibilities
  • Review and maintain familiarity with research protocols with regard to data collection.
  • Research, maintain, analyze, and abstract patient clinical trial data from pre-study background (e.g., previous diagnoses and treatments) through clinical trial participation and long-term follow-up.
  • Evaluate patient eligibility for clinical trials and assist in screening and patient enrollment.
  • Understand and interact with departments and automated systems throughout Fred Hutch/Seattle children's/UW system to ensure timely and complete delivery of data.
  • Track status of potential and active clinical trial participants.
  • Manage long-term follow-up evaluations and data collection with clinical trial participants, Fred Hutch/Seattle children's, and participants' local physicians.
  • Develop data acquisition forms and instructions for completion.
  • Manage and work with computer application specialists to ensure consistency between paper and electronic data systems.
  • Manage monitoring visits and quality control reviews by Sponsors or Investigators.
  • Support regularly scheduled institutional monitoring visits by Sponsors or Investigators to ensure quality and completeness of data.
  • Serve as a liaison and reference resource to Physicians, Investigators, other staff members, and other organizations with questions about data collection or protocol procedures and requirements.
  • Manage special projects regarding data collection, analysis, output, and presentation.
  • Provide input to support policies and goals of the program. Manage submission of reports in conjunction with the PI and Sr. Clinical Research Manager to the Human Subjects Committee, Institutional Review Board, Radiation
  • Safety Committee, Federal Drug Administration, Pharmaceutical Companies, and other agencies.
  • Liaise with Institutional Review Boards (IRB's) in submission of protocol, study amendments, annual reporting and adverse event reporting.
  • Perform other responsibilities as required.
Qualifications

MINIMUM QUALIFICATIONS:

  • Bachelor's Degree in scientific/medical field or equivalent combination of education and experience.
  • Six or more years of experience in medical records, cancer registry, clinical study coordination or related field.

PREFERRED QUALIFICATIONS:

  • Preferred Advanced Degree (Master's level or higher) in the scientific/medical field.
  • Clinical Research Associate (CRA)/ Clinical Research Professional (CRP) certification is highly desirable.
  • Strong computer skills, including proficiency in Excel and Word, and experience working with databases.
  • Strong verbal and written communication skills.
  • Knowledge of medical terminology.

The annual base salary range for this position is from $80,172 to $114,941, and pay offered will be based on experience and qualifications.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