Senior Clinical Research Coordinator — Global Trials Lead

IQVIA Inc; Columbia Township (MO); On-site; USD 44,000 - 111,000; Full time

Job summary

IQVIA seeks a Clinical Research Coordinator to support multiple trials across therapeutic areas. The role covers patient recruitment, informed consent, regulatory documentation, and site audits, with exposure to CTMS, eCRFs, and the broader clinical operations ecosystem.

You will work with investigators, sponsors and monitors, lead coordination activities, and mentor junior staff as part of a global CRO environment committed to quality and patient outcomes.

Qualifications

• Hands-on clinical skills: vital signs, phlebotomy, ECGs, lab specimens.
• Solid understanding of site operations and the drug development process.
• CRC experience (CRC I/II) with participants at a clinical site.

Responsibilities

• Manage 2–6 trials of varying complexity and lead study coordination.
• Mentor junior staff and contribute to internal training.
• Collaborate with investigators, sponsors and monitors.
• Ensure accurate documentation and timely communication.

Skills

Clinical Skills

Site Operations Knowledge

Communication & Documentation

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA seeks a Clinical Research Coordinator to support multiple trials across therapeutic areas. The role covers patient recruitment, informed consent, regulatory documentation, and site audits, with exposure to CTMS, eCRFs, and the broader clinical operations ecosystem.

You will work with investigators, sponsors and monitors, lead coordination activities, and mentor junior staff as part of a global CRO environment committed to quality and patient outcomes.