Clinical Research Associate Site Monitoring & Site Management
Listed on 2026-10-15
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist
IQVIA is seeking a Clinical Research Associate to monitor study sites in the U.S., ensuring protocol compliance and data integrity across multiple sites. You will perform monitoring visits, train site staff, and collaborate with the study team to meet timelines.
The role requires at least 2 years of on-site CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS tools. Travel and cross-functional collaboration are expected.
This role, Clinical Research Associate — On‑Site Monitoring & Site Management at IQVIA, could be your next career step.
Learn more about the Clinical Research Associate — On‑Site Monitoring & Site Management role in the description above.
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