Clinical Research Coordinator, On-Site, Bountiful, Utah
On-site · United States
Core
Coordinate clinical trials from start to finish, managing patient recruitment, informed consent, and regulatory documentation while performing clinical procedures.
Role type
Clinical Research Coordinator (CRC)
Builds
Clinical trials across multiple therapeutic areas
Domain
Clinical research / Life sciences
Required skills
Patient recruitment, informed consent, regulatory documentation, vital signs measurement, phlebotomy, ECGs, lab specimen processing, CTMS/eCRF proficiency
Responsibilities
Manage 2–6 trials of varying complexity, perform clinical procedures, lead study coordination from start to finish, work closely with investigators and sponsors, mentor junior staff
Seniority
Mid-level (1-3 years for CRC I, 3+ years for CRC II)