Clinical Research Coordinator, On-Site, Bountiful, Utah
IQVIA · Bountiful, UT, United States of America · Global
Clinical Research
–
Not yet analysed
Demand78
Career growth70
Healthcare fit74
Remote potential10
5-year outlook
Clinical research coordination experience can lead into senior CRC, site management, clinical trial management, or sponsor/CRO roles. Compensation growth depends on trial complexity, certifications, and progression into management or monitoring.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
–
Date found
2026-10-24
Intelligence details
Flexible work details
- Eligible countries
- United States
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for clinicians interested in clinical trials and research operations, especially those seeking a structured entry point into CRO/site work. The lack of a detailed description means applicants should verify experience requirements, trial portfolio, and on-site expectations before applying.
Who should apply
Nurses, allied health professionals, pharmacists, IMGs, and healthcare graduates with an interest in clinical trials, research compliance, and patient-facing study coordination. Doctors considering a non-clinical research pathway may also find it relevant.
CV angle
Reframe real clinical experience around trial-adjacent strengths: patient screening and scheduling, informed consent discussions, protocol adherence, accurate documentation, data entry, regulatory compliance, multidisciplinary teamwork, and handling sensitive participant information. Do not claim trial coordination experience unless genuine.
Skills to highlight
- Clinical trial coordination
- Informed consent
- Protocol adherence
- Data collection and documentation
- Regulatory compliance
- Patient scheduling and follow-up
- GCP principles
- Multidisciplinary teamwork
Role summary
An on-site Clinical Research Coordinator role at IQVIA in Bountiful, Utah, focused on supporting clinical trial site operations, participant coordination, data collection, and regulatory documentation.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.