Job Description

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

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