Senior Research Coordinator
IQVIA · Lexington, KY +1 more
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Role summary
IQVIA seeks a Senior Research Coordinator for its Site Management Organization in Lexington, Kentucky. The role involves managing multiple clinical trials across therapeutic areas, performing clinical procedures, and coordinating study activities from recruitment through regulatory documentation. Candidates should have 3+ years of clinical research experience at an investigative site, proficiency with clinical trial systems, and strong communication skills.
What they're looking for
- 1–3 years clinical research experience at investigative site (CRC I level)
- Phlebotomy, vital signs, ECG, and lab specimen processing skills
- Knowledge of site operations and drug development processes
- Strong written and verbal communication with meticulous attention to detail
- Proficiency with CTMS, eCRFs, and Microsoft Office applications
What you'll be doing
- Manage 2–6 concurrent trials across varying complexity levels
- Execute study coordination activities including patient recruitment and informed consent
- Maintain regulatory documentation and prepare for site audits
- Mentor junior staff and contribute to internal training programs
- Collaborate with investigators, sponsors, and monitors on trial activities
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.