Clinical Research Associate: Site Monitor & Study Manager
Listed on 2026-10-18
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Research/Development
Clinical Research
IQVIA is seeking a Clinical Research Associate to monitor study sites and manage data reporting in compliance with protocol, GCP and ICH guidelines. The role involves coordinating with sites, training staff, and tracking regulatory submissions throughout the study lifecycle.
The position requires 2+ years of on-site CRA experience, strong communication skills, and proficiency with EDC/CTMS/eTMF systems. This is a US-based opportunity with a focus on quality and accountability.
The Clinical Research Associate:
Site Monitor & Study Manager position in the Bio & Pharmacology & Health field is open for applications.
For the Clinical Research Associate:
Site Monitor & Study Manager position at IQVIA, we are reviewing applications now.
Step into the Clinical Research Associate:
Site Monitor & Study Manager role at IQVIA in Camden, NJ, United States and grow with us.
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