Clinical Research Associate Jobs in Utah, United States

The FSP team seeks a Clinical Research Associate 2 to support clinical trials on the West Coast or in Texas. This role involves comprehensive site monitoring, data integrity verification, and adverse event reporting to ensure participant safety and protocol compliance.

Evolution Research Group seeks a Contract Senior Clinical Research Associate in Utah to conduct site monitoring for clinical trials. The role involves independently managing site qualification, initiation, interim monitoring, and close-out visits while ensuring compliance with FDA regulations and ICH guidelines.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, Psychiatry, manages site activities from start‑up through close‑out, conducts initiation visits, ensures regulatory compliance, and supports safety reporting, primarily remotely with regional travel on the West Coast.

Clinical Operations at Worldwide Clinical Trials drives innovative therapeutic research across neuroscience and psychedelics. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, ensures regulatory compliance, and supports contract and budget negotiations.

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.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, and ensures regulatory compliance for CNS and Psychiatry trials.

Join a global clinical research team that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

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.

Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Associates (CRA 1) for Oncology, CAR T, or Ophthalmology trials. The role involves site monitoring, data integrity verification, SAE reporting, and supporting study site operations across Central or West coast US hubs or Montreal, Canada.

Clinical Research Coordination team at Tanner Memorial Clinic manages trial subject recruitment, consent, screening, and compliance. The role coordinates trial activities, generates source documents, handles visit scheduling, product dispensing, data collection, phlebotomy, and AE reporting while communicating with sponsors and authorities.

Rocky Mountain Multiple Sclerosis Clinic seeks a Clinical Research Coordinator to manage Neurology studies, ensuring trial integrity and patient safety. The role handles EDC data entry, scheduling, vital signs, blood draws, ECGs, and serves as primary contact for subjects and sponsors.

This is a fully on-site position in Bountiful, Utah Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands‑on responsibilities, and a collaborative team environment.

Clinical Research Coordinator, Non-RN in the Information Technology Services department at University of Utah Health. Coordinates day-to-day clinical research activities, including screening, consenting, scheduling visits, maintaining patient and laboratory data, and ensuring compliance with GCP, IRB, FDA and other regulations.

ThermoFisher Scientific's PPD clinical research portfolio seeks a Traveling Research Associate II to support clinic operations, manage patient care workflows, and ensure regulatory compliance across clinical trial sites. Day-to-day duties include performing technical and non-technical clinic procedures (vital signs, phlebotomy, urine collection, sleep testing), preparing and calibrating equipment, managing clinical supplies and specimen documentation, screening subjects per protocol, liaising wi

Research Team at doTERRA International focuses on ensuring product safety through scientific evaluation. The Associate Research Scientist II conducts safety assessments, literature reviews, and supports cross‑functional collaborations to evaluate chemistry and toxicological data.

Satisfaction Research Center at Activated Insights improves senior care experiences through surveys and technology. As an Associate you conduct phone surveys, accurately document feedback, and create positive experiences for participants to help organizations enhance care and employee satisfaction.

Elsevier Clinical Content Team creates evidence‑based nursing reference material. The Associate Clinical Editor reviews, updates, and revises assigned content, ensures accuracy to clinical guidelines, and collaborates with internal teams to address content needs.

Clinical Territory Associate on the UT/ID team at Intuitive Surgical, advancing robotic-assisted surgery through clinical support and territory development. Partners with sales reps to train surgeons, guide technical in‑services, and promote advanced technology to existing robotic users while managing reporting and administrative tasks.

Elsevier Clinical Content Team builds and maintains evidence‑based nursing reference material. The Associate Clinical Editor reviews, updates and revises assigned content, ensures accuracy to current practice guidelines, and manages project timelines while collaborating with internal teams and responding to clinical inquiries.

Rocky Vista University (RVU) seeks an Associate Dean of Clinical Education, RVUCOM to lead the Department of Clinical Education and oversee clinical training years for its osteopathic medical program. The role drives program development, osteopathic curriculum delivery and assessment, clinical site and preceptor recruitment, budget management, and student career/residency advising (NRMP Match, ERAS, Residency CAS).