Clinical Research Associate - Site Monitoring & Management
Listed on 2026-10-15
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Research/Development
Research Assistant/Associate, Clinical Research
IQVIA is seeking a Clinical Research Associate (CRA) to perform site monitoring and data reporting across assigned U.S. sites.
You will ensure study protocol adherence, regulatory compliance, and data integrity per GCP guidelines, with responsibility for monitoring visits, communications, and recruitment tracking. Experience with EDC, CTMS, and eTMF is preferred, as is strong English communication and organizational skills.
This is a genuine opportunity to take on the Clinical Research Associate
- Site Monitoring & Management 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 & Management role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
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