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.

Clinical team at Eupraxia Pharma focuses on advancing locally delivered, extended‑release therapeutics using the DiffuSphere™ platform. The Clinical Research Associate supports trial operations by overseeing site monitoring, managing CRO partners, training staff, and ensuring compliance with FDA/ICH‑GCP standards.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

Clinical Research Associate II on the Oncology & Neurology team at Thermo Fisher Scientific. The role monitors investigator sites, ensures protocol compliance, manages data accuracy, and coordinates audit readiness across multiple states.

PPD Development, LP’s Clinical Research Associate team drives global clinical trials, ensuring protocol compliance and data integrity. The role monitors investigator sites, conducts risk‑based monitoring, and manages documentation across 100+ countries.

Clinical Research Associate (Level II) at Thermo Fisher Scientific supports clinical trials across 100+ countries, monitoring sites 50% onsite and 50% remote. Responsibilities include risk‑based monitoring, data verification (SDR, SDV, CRF), protocol compliance, audit readiness, investigator communication, and reporting to the Clinical Team Manager.

Thermo Fisher Scientific seeks a Clinical Research Associate (Level II) to monitor clinical trials across multiple U.S. sites. The role blends on‑site and remote visits, applying risk‑based monitoring, ICH‑GCP compliance, and data accuracy checks (SDR, SDV, CRF).

Senior Clinical Research Associate overseeing site performance and compliance for oral healthcare studies, ensuring safety, efficacy, and regulatory standards. Drives process improvements, collaborates with cross‑functional teams, supports study managers, and contributes to database UAT, CTMS maintenance, and audit readiness.

Pediatric BMT/Immunotherapy Research Associate at Fred Hutchinson Cancer Center in Seattle, Washington. The role is a 12‑month fellowship focused on pediatric hematopoietic cell transplantation and immunotherapy, rotating through outpatient and inpatient transplant services while gaining independent patient care responsibility.

We are seeking an experienced Oncology Clinical Research Associate (CRA) to lead and support our full-service outsourcing team. The role focuses on site monitoring, data integrity, SAE reporting, and regulatory compliance for CAR‑T trials.

Cardiothoracic Surgery at Washington University in St. Louis invites a postdoctoral researcher to join an NIH‑funded lab focused on immunometabolism in lung fibrotic disease. The role involves independent studies on human and mouse tissues, advancing a human lung chip, and publishing high‑impact papers.

Providence Swedish Research team advances neuroscience studies by coordinating clinical research and supporting investigators. The Associate Clinical Research Coordinator independently manages study tasks, handles budgeting and billing, and backs up peers, ensuring smooth study operations.

Tumor Institute Research at Providence Swedish coordinates clinical studies to advance cancer care. The Associate Coordinator independently manages study logistics, data collection, and regulatory compliance while supporting investigators and budgeting.

Associate Director Clinical Research - Pediatrics Central Administration leads the Pediatric Clinical Research Unit (PCRU) at Washington University Medical Campus, overseeing day‑to‑day operations, staff recruitment, training, and performance. The role develops and implements policies, monitors financial performance, ensures compliance with IRB, federal mandates, and industry standards, and supports strategic planning.

Department of Psychiatry Clinical Research Infrastructure team builds and sustains a department-wide program to collect standardized clinical data, patient-reported information, biospecimens, and biomarkers. The Associate Director leads protocol development, workflow design, governance, and quality improvement while supervising staff and managing budgets.

Fred Hutch Clinical Biorepository team supports scientific research by managing clinical research specimens with strict chain of custody. The associate accessiones specimens, maintains electronic inventory, performs data entry, supports quality assurance reporting, and assists with routine lab operations such as freezer maintenance and supply management.

Fred Hutchinson Cancer Research Center’s Gastrointestinal Oncology team delivers world‑class ambulatory care for GI malignancies while advancing cutting‑edge research trials. The role blends clinical service, teaching of trainees, and participation in clinical research and trial patient recruitment at the South Lake Union campus.

Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch provides statistical and data management support for HIV prevention clinical trials. The associate delivers intermediate-level statistical analysis, power calculations, data management, and documentation across trial phases while mentoring junior staff.

SCHARP at Fred Hutchinson Cancer Center, the hub for HIV/AIDS clinical trial statistics, seeks a Statistical Research Associate II/III to design power calculations, develop randomization lists, and produce SAS/R analysis datasets for phase I‑III studies. The role collaborates with statisticians, data managers, and investigators to draft protocols, statistical analysis plans, and CDISC‑compliant reports, while mentoring junior SRAs and driving quality assurance initiatives.

Pharmacy Research team at Seattle Children’s Hospital provides technical support for pharmaceutical research, ensuring safe preparation of sterile and non-sterile medications. The associate follows established procedures, handles investigational drug processes, and supports Good Clinical Practice compliance.