Clinical Research Associate - On-Site Monitoring Expert
Listed on 2026-10-13
-
Research/Development
Clinical Research, Research Assistant/Associate -
Healthcare
Clinical Research
IQVIA is seeking a Clinical Research Associate to join our global clinical operations team. The role involves performing site monitoring visits, ensuring data quality and regulatory compliance across trials, and supporting site performance with training and communication.
You will manage site relationships, track recruitment and data flow, and help maintain documentation in the TMF. A Bachelor’s degree and 2+ years on-site CRA experience are preferred.
For the Clinical Research Associate
- On-Site Monitoring Expert position at IQVIA, we are reviewing applications now.
The following opening is for a Clinical Research Associate
- On-Site Monitoring Expert with IQVIA.
Our group is growing, and we are hiring a Clinical Research Associate
- On-Site Monitoring Expert in O'Fallon, IL, United States.
This opening is for the Clinical Research Associate
- On-Site Monitoring Expert role at IQVIA.
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