Clinical Research Coordinator, On-Site
IQVIA · Kansas City, MO
Clinical OperationsFull-time$38k–$95kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Coordinator position at an on-site SMO managing 2–6 concurrent trials. The role involves patient recruitment, informed consent, regulatory documentation, clinical procedures, and coordination activities. Candidates need 1–3 years (CRC I) or 3+ years (CRC II) of clinical research experience, clinical skills in vital signs and phlebotomy, and proficiency with CTMS and eCRF systems.
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.