Clinical Research Associate Jobs in Oregon, 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 seeking a Clinical Research Associate 2 for the West Region to deliver high-standard clinical trial monitoring and participant care across the western United States. Day-to-day work includes full-cycle site monitoring (routine and close-out visits, pre-study/initiation visits, study file maintenance), CRF review and query resolution, SAE reporting, registry management, and acting as a local project coordinator or client contact.

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.

Join the Knight Cancer Institute and play a key leadership role in a large NIH-funded clinical trial focused on improving the health and quality of life of cancer survivors. We are seeking a highly organized and motivated Clinical Research Associate (Project Director) to lead the day-to-day operations of a supportive care clinical trial.

The Clinical Research Coordinator I will function under the supervision of the Clinical Trials Manager. Coordinates and maintains diverse activities in the conduct of clinical research trials related to heart and vascular research.

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.

The CRA II assists in the execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This position works with confidential patient and company data, and interfaces with a variety of internal and external stakeholders.

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.

Join us as a Clinical Research Associate II/Sr. Clinical Research Associate I- Make an impact at the Forefront of Innovation.

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.

TI Clinical Research Coordinator at Oregon Health & Science University’s Knight Cardiovascular Institute (KCVI) supports the Clinical Trials Unit’s mission to advance cardiovascular treatments. The role coordinates patient visits, data entry, and regulatory documentation for cardiomyopathy studies, working closely with study coordinators and monitoring teams.

Epilepsy Division, Department of Neurology at Oregon Health & Science University conducts cutting‑edge therapeutic trials for epilepsy. The Senior Clinical Research Assistant coordinates complex interventional studies, prepares IRB submissions, manages participant recruitment, and handles sample processing and data entry.

Headlands Research Clinical Research team advances new therapies by managing patient-focused clinical trials across a growing network of sites. Coordinators support day-to-day trial execution, including patient interactions, study visit scheduling, data collection, and regulatory compliance while collaborating with investigators and cross‑functional teams.

Headlands Research Clinical Research team supports clinical trial delivery across community sites, leveraging technology and support services to expand patient participation. Clinical Research Assistants help execute trials by assisting with study visits, preparing materials, collecting and organizing data, and ensuring protocol compliance while interacting directly with patients and care teams.

Science 37’s Nursing Solutions Group seeks a Per Diem Mobile Research Nurse to deliver home-based clinical care for clinical trials. The role involves providing nursing services at participants’ homes, applying research and nursing practices, collaborating with lead nurses, supporting operational development, and serving as a subject matter expert.

The Clinical Research Budgets Analyst will be responsible for the timely and accurate preparation and maintenance of budget templates for sponsored clinical trials, including the comparative review against budgets offered by study sponsors and the set-up of study payments milestones in the Clinical Trial Management System.

The HEAL thy B rain and C hild D evelopment (HBCD) Study at OHSU is conducting studies with pregnant people and their children in the areas of neurodevelopment, behavior, learning, environmental factors, substance exposure, and cognitive functioning under the direction of Principle Investigators, Alice Graham, Ph.D. and Elinor Sullivan, Ph.D. We have an opening for an energetic and highly motivated full-time Clinical Research Assistant.