Job Description

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.

Responsibilities

• 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

Requirements

• 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

Compensation: $37,800–$94,500 base annually

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