Clinical Research Associate Jobs in Washington, United States

The Associate Clinical Research Coordinator (CRC1) role within the RESEARCH team coordinates and maintains diverse activities related to clinical cancer research in Kennewick, WA, United States. Day-to-day responsibilities include managing patient eligibility, enrollment, data compilation and submission, study evaluation, quality control, and patient follow-up.

The Clinical Research Associate II at AbbVie advances the company's pipeline by conducting clinical research monitoring and ensuring trial compliance, data integrity, and patient safety across immunology, oncology, neuroscience, and Allergan Aesthetics therapeutic areas. Day-to-day, the role serves as the primary site contact, conducting site evaluations, routine and closure monitoring, training site staff and principal investigators, managing investigator payments, and mentoring less experience

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

Clinical Pathology/IHC Biomarker Development team at SystImmune focuses on creating and validating immunohistochemistry assays for cancer biomarker programs. The Research Associate supports assay optimization, performs tissue sectioning and automated IHC staining, and documents results in ELN/LIMS systems.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

The Clinical Research RN - Oncology Research role at Swedish Edmonds independently coordinates research and administrative tasks across multiple study locations, working with investigators and a supervisor to resolve study-related issues and back up other coordinators. Day-to-day duties include supporting department financial performance through budgeting and billing, developing specialized research instruments, and assisting with scientific manuscripts or presentations, with possible after-hour

Clinical Research Coordinator I (Clinic) – Medical Oncology at Washington University in St. Louis is responsible for screening, enrolling, and coordinating patients in oncology clinical trials. The role manages all phases of study protocols, ensuring compliance with regulatory guidelines, maintaining accurate record‑keeping, and reporting adverse events.

The Heart Research team seeks a Clinical Research Coordinator or Senior Clinical Research Coordinator to support clinical trials in Seattle, WA. The role involves day-to-day research coordination, budgeting, and billing activities on-site. Candidates must have 3-5 years of experience and hold a Bachelor's degree or equivalent significant experience.

MultiCare Health System's Clinical Research team advances patient care through rigorous clinical studies. The Clinical Research Coordinator I implements basic science and phase II‑IV trials, manages study documentation, specimen processing, and coordinates monitor visits.

Infectious Disease Sciences Program at Fred Hutchinson Cancer Center supports vaccine and infectious disease research. The Clinical Research Coordinator I assists with planning, implementing, and closing industry-sponsored clinical trials and observational studies, handling regulatory documentation, data collection, and patient coordination.

Advanced Therapeutics - Liquid Malignancy Team (Leukemia & Lymphoma) at Seattle Children’s Hospital advances pediatric cancer treatments. The Coordinator supports clinical trial organization, regulatory compliance, and protocol implementation, working closely with the Principal Investigator.

Clinical Research Support at Fred Hutchinson Cancer Center focuses on advancing oncology trials through rigorous monitoring and quality assurance. The Clinical Research Monitor II independently conducts routine and for‑cause monitoring of investigator‑initiated oncology trials, documents observations, and collaborates with investigators to resolve findings and improve study conduct.

CTMS Program Office at Fred Hutchinson Cancer Center builds and configures study calendars and financials in the OnCore Clinical Trial Management System to support clinical research. The analyst interprets protocols, configures electronic study calendars and budgets, performs quality assurance, and provides superior customer service to research teams and end users.

Fred Hutchinson Cancer Center seeks a Clinical Research Coordinator II for its Phase 1 Clinical Trial Program in Seattle, WA. This role manages day-to-day oncology trial operations, including patient screening, visit coordination, and regulatory documentation. The position is full-time with an on-site work model at the South Lake Union campus.

The Cruchaga lab at the NeuroGenomics and Informatics Center hires a Clinical Research Coordinator III to oversee complex multi‑site studies, manage regulatory compliance, and supervise research staff. The role coordinates protocol development, data analysis, and manuscript preparation while ensuring IRB and sponsor requirements are met.

Clinical Research Support Services at Fred Hutchinson Cancer Center coordinates interventional Phase I-III clinical trials and observational cancer control studies. The coordinator manages patient screening, enrollment, visit scheduling, specimen collection, data abstraction, and regulatory compliance on a daily basis.

Clinical Research Support team at Fred Hutchinson Cancer Center coordinates interventional Phase I-III trials and cancer control studies to advance oncology research. The Coordinator manages patient screening, enrollment, visit scheduling, specimen collection, data abstraction, and regulatory compliance, collaborating with Data Coordination staff and specialized Oncology teams.

Seattle Children’s seeks a Clinical Research Budget Analyst to develop and negotiate complex clinical trial budgets and coverage analyses for industry sponsors and grants. The role involves building internal cost models, leveraging CTMS systems, and guiding junior colleagues to improve research workflows.

Tasso Clinical team develops at-home diagnostic testing solutions to improve patient access and data quality. The Clinical Research Coordinator 2 conducts study visits, collects specimens, manages data entry in EDC systems, and supports protocol compliance across multiple sites.

Precision Oncology Clinical Research Coordinator II at Fred Hutchinson Cancer Center, supporting the Stuart and Molly Sloan Precision Oncology Institute. Coordinates investigator-initiated and industry-sponsored studies, handling patient screening, enrollment, specimen collection, and documentation while ensuring compliance with protocols and regulations.