Clinical Research Coordinator, On-Site, Bountiful, Utah
IQVIA · Bountiful, UT
Clinical OperationsFull-time$37k–$91kCompany career page
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Role summary
This fully on-site clinical research coordinator role in Bountiful, Utah involves managing multiple trials of varying complexity, performing clinical procedures, and overseeing study coordination activities. The position requires 1–3 years of clinical research experience for CRC I level or 3+ years for CRC II level, along with proficiency in vital signs, phlebotomy, ECGs, and electronic data systems.
What they're looking for
- 1-3 years clinical research experience at investigative site (CRC I level)
- Proficiency obtaining vital signs, phlebotomy, ECGs, specimen processing
- Strong written and verbal communication with meticulous attention to detail
- Solid understanding of site operations and drug development processes
- Competency with CTMS, eCRF systems, and Microsoft Office applications
What you'll be doing
- Manage 2-6 concurrent trials of varying complexity and therapeutic areas
- Conduct patient recruitment, informed consent, and regulatory documentation
- Perform clinical procedures including vital signs, phlebotomy, and ECG administration
- Coordinate study activities from initiation through completion and site audits
- Mentor junior staff and contribute to internal training initiatives
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.