Clinical Research Associate: Site Monitoring & Coordination
Listed on 2026-10-16
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking an on-site Clinical Research Associate (CRA) to monitor study sites, ensure protocol compliance, and support data integrity. The role requires coordinating with sites, managing recruitment plans, and maintaining regulatory documentation in line with GCP and ICH guidelines.
The candidate should have at least 2 years of independent on-site CRA experience, strong English communication, and proficiency with EDC/CTMS/eTMF/IVRS/IWRS.
This is a strong opening to take on the Clinical Research Associate:
Site Monitoring & Coordination role at IQVIA.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Research Associate:
Site Monitoring & Coordination role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
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