Clinical Research Associate Jobs in Utah, United States

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 PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

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 Research team at bioMérieux leads the execution of global clinical evidence generation programs, designing and managing studies from protocol to final report. The Clinical Research Scientist drives study planning, budget and timeline management, oversees site operations, data integrity, regulatory compliance, and mentors associate scientists.

We are excited to announce that in partnership with our client, we are currently looking for a District Sales Manager to join our team. The District Sales Manager will lead and inspire a field-based sales team that capitalizes on local market potential, customer needs, and market access dynamics, to meet & exceed business goals.

The Department of Veterinary Clinical and Life Sciences at Utah State University’s College of Veterinary Medicine seeks a faculty member to teach and advance veterinary anesthesia and analgesia in the new DVM curriculum. The role involves delivering hands‑on instruction, developing innovative teaching methods and assessments, and optionally leading a research program and service on committees.

College of Veterinary Medicine, Department of Veterinary Clinical & Life Sciences at Utah State University seeks an Assistant, Associate, or Full Professor of Large Animal Surgery to lead surgical instruction in the new DVM curriculum, develop innovative teaching methods, and contribute to curriculum design. The role involves delivering hands‑on large animal surgery labs, mentoring students, and optionally building a nationally recognized research program with external funding.

Utah State University seeks an experienced veterinary professional to serve as Assistant, Associate, or Full Professor of Large Animal Internal Medicine. The role blends teaching, curriculum development, and optional research within the College of Veterinary Medicine.

Program Assistant at University of Utah Health supports program administration and development across clinical and non‑clinical departments. The role involves planning and implementing programs, compiling and organizing data for database entry, distributing program information, and conducting research.

This fully on-site Clinical Research Coordinator role at IQVIA in Springville, Utah involves coordinating and participating in clinical studies, ensuring compliance with protocols, GCP, and sponsor SOPs. Responsibilities include patient recruitment, consent, scheduling, data entry, inventory management, and supporting study visits and monitoring.

Clinical Research team at doTERRA International focuses on advancing scientific studies to support product efficacy. As a Clinical Research Intern I you will collaborate on new research project ideas, assist in study design, write proposals and reports, and process biological samples while analyzing data.

doTERRA International seeks a motivated and detail-oriented Clinical Research Coordinator to support its expanding portfolio of clinical and pre‑clinical research initiatives. The role is ideal for early‑career professionals or students nearing graduation in life sciences who are passionate about wellness, natural products, and evidence‑based research.

This is a fully on-site position in Salt Lake City, Utah. Are you ready to accelerate your career in clinical research?

CenExel Clinical Research RN (Day Shifts) supports the execution of clinical studies by providing patient care, managing study protocols, and serving as the primary liaison with sponsors. The RN conducts nursing assessments, documents data, screens and schedules participants, and ensures regulatory compliance in a fast‑paced clinic 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.

Clinical Research Coordinator II at Shriners Hospitals for Children in Salt Lake City, Utah. The role ensures compliance and oversight of pediatric clinical studies, coordinating protocols, IRB submissions, recruitment, and data management.

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.

Clinical Research Neurologist (Principal Investigator) at Nira Medical’s Rocky Mountain MS Clinic in Salt Lake City. The role builds outpatient neurology care while leading industry-sponsored clinical trials, overseeing study conduct, patient safety, and data integrity.

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 – On‑site in Bountiful, UT. Join Avacare, a dynamic Site Management Organization (SMO) under IQVIA, to coordinate 2–6 clinical trials, perform vital signs, phlebotomy, ECGs, and lab specimen processing, and manage study coordination from start to finish. Work closely with investigators, sponsors, monitors, and mentor junior staff.