Clinical Research Associate Jobs in Washington, United States

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.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Assist in the organization, implementation, and completion of clinical research studies in compliance with all applicable laws and regulations, institutional/ departmental guidelines, standards of Good Clinical Practice (GCP), and within budget. Create, collect, and review study-related documents.

The Senior In-house Clinical Research Associate (Sr. IHCRA) provides hands-on support for the day-to-day execution of clinical trial activities as assigned by Clinical Project Delivery (CPD) and/or Clinical Site and Trial Operations (CSTO).

Prepares, facilitates, coordinates, and submits documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be require

Fortrea is seeking Experienced CRA 2s to lead and support its Full Service Outsourcing team across major US hub locations. In this role, you will apply clinical judgement to monitor clinical trial sites, ensure participant safety and data integrity, and respond to emergencies per clinical research standards.

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

The FSP team at Covance is seeking a Sr. CRA 2 to provide high-standard clinical trial care and respond to emergency situations based on clinical research standards. Day-to-day responsibilities include all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaising with vendors, and other duties as assigned.

The Sr. CRA II - General Medicine - East Coast or Mid-West role supports the Full Service Outsourcing team at Covance, reporting within the Fortrea Inc. organization. You will lead and support clinical trial operations by performing all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.

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.

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.

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.

The Clinical Research Coordinator II supports quality clinical research at assigned investigative sites in Seattle, WA, ensuring studies follow sponsor protocols, FDA regulations, and ICH/GCP guidelines while delivering high-quality data to sponsors. Day-to-day, the role conducts subject visits and protocol-required procedures, manages data entry and query resolution, coordinates with laboratory, data, administrative, investigator, participant, and sponsor/CRO teams, oversees adverse event repor

Fred Hutchinson Cancer Center in Seattle, WA is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. The Bilingual Clinical Research Coordinator I supports a health-focused research study testing lifestyle, behavioral, and nutritional education interventions on clinical and quality of life outcomes in cancer survivors.

Clinical Research Coordinator II at Fred Hutchinson Cancer Center in Seattle, WA. The role manages day‑to‑day operations of oncology clinical trials for the Immunotherapy Integrated Research Center, coordinating patient enrollment, visits, data entry, and regulatory compliance. It requires strong organizational skills, GCP knowledge, and collaboration with clinical teams, and is based on the South Lake Union campus with on‑site work.

Fred Hutchinson Cancer Center's Clinical Research Coordinator I supports the day-to-day operations and administrative functions of hematopoietic cell transplantation observational studies focused on survivorship. The coordinator screens patients for eligibility, tracks visits, coordinates clinic procedures, and collects, abstracts, reports, and quality-controls study data under IRB-approved protocols, while also managing long-term follow-up activities.

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.

The Clinical Research Coordinator II at Fred Hutchinson Cancer Center coordinates interventional Phase I-III clinical trials and observational Cancer Control studies within specialized Oncology research teams, including Nuclear Medicine and Neurology. Day-to-day work includes screening patients for eligibility, performing enrollments, tracking patient visits, abstracting and reporting study data, coordinating research specimen collection and submission, and creating and maintaining research docu