Clinical Research Associate: On-site Monitoring
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking a Clinical Research Associate to monitor study sites in compliance with the protocol, ICH/GCP, and sponsor requirements. You will manage site visits, ensure data quality, and track regulatory submissions.
The ideal candidate has 2+ years of on-site CRA experience, strong regulatory knowledge, and excellent communication and problem-solving skills. The role requires working with sites and coordinating documentation and data queries.
This opportunity is for the Clinical Research Associate:
On-site Monitoring role at IQVIA.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Clinical Research Associate:
On-site Monitoring role at IQVIA, based in West Point, MS, United States.
We are looking to fill the Clinical Research Associate:
On-site Monitoring position at IQVIA in West Point, MS, United States.
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