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Clinical Research Associate Bridge Program Jobs in Seattle, WA

The Research Associate, Analytical Sciences will support drug substance and drug product ... including clinical and commercial programs, with emphasis on biologics identity, purity ...

... program, and broadly by hospital systems across the US. We are looking for a Clinical Research ... This position will report to our Associate Director, Clinical Operations. An ideal candidate will ...

... program, and broadly by hospital systems across the US. We are looking for a Clinical Research ... This position will report to our Associate Director, Clinical Operations. An ideal candidate will ...

... program, and broadly by hospital systems across the US. We are looking for a Clinical Research ... This position will report to our Associate Director, Clinical Operations. An ideal candidate will ...

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Clinical Research Associate Bridge Program information

See Seattle, WA salary details

$13

$46

$79

How much do clinical research associate bridge program jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical research associate bridge program in Seattle, WA is $46.80, according to ZipRecruiter salary data. Most workers in this role earn between $32.84 and $59.90 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate in a bridge program?

To thrive as a Clinical Research Associate in a bridge program, you need a foundational understanding of clinical trials, regulatory compliance, and data management, usually supported by a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, effective communication, and organizational skills help you manage study protocols and collaborate with diverse teams. These competencies are crucial for ensuring clinical trial integrity, regulatory adherence, and the successful execution of research studies.

What types of mentorship and training can I expect in a Clinical Research Associate Bridge Program?

Participants in a Clinical Research Associate (CRA) Bridge Program typically receive structured mentorship from experienced CRAs and clinical research professionals. The program often includes hands-on training in protocol review, site monitoring, regulatory compliance, and data management, combined with classroom or online learning modules. You'll work closely with cross-functional teams, such as clinical project managers and regulatory specialists, gaining exposure to industry-standard processes and tools. This supportive environment is designed to accelerate your transition into a CRA role and help you build a strong professional network within clinical research.

What is a Clinical Research Associate Bridge Program?

A Clinical Research Associate (CRA) Bridge Program is a specialized training course designed to help individuals transition into the role of a CRA, especially those with related experience in healthcare, life sciences, or clinical research support. These programs typically combine classroom instruction with practical training, focusing on topics such as clinical trial monitoring, regulatory compliance, and Good Clinical Practice (GCP) guidelines. The goal is to equip participants with the necessary knowledge and skills to begin a career as a CRA, often including job placement assistance or internships. Bridge programs are ideal for those who want to move into clinical research from a related field but lack direct CRA experience.
What are popular job titles related to Clinical Research Associate Bridge Program jobs in Seattle, WA? For Clinical Research Associate Bridge Program jobs in Seattle, WA, the most frequently searched job titles are:
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Infographic showing various Clinical Research Associate Bridge Program job openings in Seattle, WA as of June 2026, with employment types broken down into 52% Full Time, 39% Part Time, 8% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $97,349 per year, or $46.8 per hour.

$97K - $146K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 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 Monitor II supports the quality and regulatory compliance of investigatorinitiated oncology clinical trials conducted within the Cancer Consortium. This role performs remote monitoring activities on behalf of the institution to ensure research is conducted in accordance with protocol requirements, Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements. The Clinical Research Monitor partners closely with investigators, research coordinators, data managers, and regulatory staff to promote data integrity, participant safety, and continuous quality improvement across the clinical research portfolio. This role reports to the Assistant Director of Clinical Research Monitoring within Clinical Research Support (CRS).

Most Fred Hutch jobs require some on-campus work. However, there may be flexibility for certain positions. Please check with the recruiter if you are an out-of-state applicant interested only in working outside of the Seattle area.

Responsibilities
  • Independently conduct routine and forcause monitoring of oncology clinical trials.
  • Manage several priorities within multiple complex trials.
  • Document monitoring observations, prepare written reports, and oversee issues through resolution.
  • Apply seasoned judgment to identify compliance risks and trends; escalate concerns as appropriate.
  • Work collaboratively with Principal Investigators and study teams to resolve findings and improve study conduct, including supporting the development of corrective and preventive actions (CAPAs).
  • Contribute to the development, refinement, and maintenance of standard operating procedures (SOPs), tools, and templates.
  • Participate in institutional research quality initiatives and process improvement efforts.
  • Support onboarding, mentoring, and co-monitoring by modeling best practices and reinforcing quality expectations.
  • Other duties as assigned.
Qualifications

MINIMUM QUALIFICATIONS:

  • Bachelor's or advanced degree.
  • Strong knowledge of clinical research with exceptional written, verbal, and interpersonal skills.
  • Minimum of 7+ years of experience in clinical research monitoring (oncology experience preferred).

PREFERRED QUALIFICATIONS:

  • In-depth knowledge of FDA regulations, GCP guidelines, and other relevant regulatory requirements governing clinical trials.
  • Experience with electronic data capture (EDC) systems and electronic regulatory platforms.
  • Effectively partners with crossfunctional teams and external stakeholders to support study goals.
  • Excellent organizational, analytical, and problem-solving abilities.
  • Clinical research-related certification.
  • Experience working in an NCI-designated cancer center or academic consortium environment.

The annual base salary range for this position is from $97,822 to $146,681, 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