Clinical Research Coordinator
IQVIA · Tempe, AZ
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Role summary
IQVIA seeks a Clinical Research Coordinator for an on-site position in Tempe, Arizona. The role involves managing multiple clinical trials, performing clinical procedures, and coordinating study activities from recruitment through regulatory documentation at a Site Management Organization.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-06). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- 1–3 years clinical research experience at investigative site (CRC I level)
- Proficiency obtaining vital signs, phlebotomy, ECGs, and specimen processing
- Strong written and verbal communication with meticulous attention to detail
- Experience with CTMS, eCRF systems, and Microsoft Office
- Understanding of site operations and drug development processes
What you'll be doing
- Manage 2–6 clinical trials of varying complexity and therapeutic areas
- Conduct patient recruitment, informed consent, and ongoing participant engagement
- Prepare and maintain regulatory documentation, study files, and audit readiness
- Collaborate with investigators, sponsors, and monitors on trial execution
- Support junior staff through mentoring 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.