Clinical Research Coordinator

IQVIA seeks a Clinical Research Coordinator for an on-site position in Las Vegas to manage multiple clinical trials at varying complexity levels. The role offers exposure to diverse therapeutic areas, regulatory documentation, patient recruitment, and site operations within a collaborative SMO environment backed by global CRO resources.

Responsibilities Manage 2–6 concurrent trials of varying complexity from initiation through completion Lead patient recruitment, informed consent processes, and regulatory documentation activities Perform clinical procedures and coordinate study activities with investigators, sponsors, and monitors Support site audits and contribute to internal staff training and mentoring initiatives Requirements 1–3 years clinical research experience at investigative site (CRC I level) or 3+ years as Clinical Research Coordinator (CRC II level) Hands-on proficiency obtaining vital signs, phlebotomy, ECG administration, and lab specimen processing Solid understanding of site operations and drug development processes Strong written and verbal communication with meticulous attention to detail and time management Proficiency with CTMS, eCRF systems, and Microsoft Office applications Compensation:

$40,800–$102,000 base annually