Clinical Research Associate - Site Monitoring Pro
Listed on 2026-10-17
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist
IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data integrity in line with the protocol, GCP, and sponsor requirements.
Responsibilities include site visits, recruitment tracking, protocol training, and maintaining TMF/ISF documentation while collaborating with the study team. A BA/BS in a scientific field and 2+ years on-site CRA experience are preferred.
The Clinical Research Associate
- Site Monitoring Pro role at IQVIA is now open for applications in Ontario, CA, United States.
We invite applications for the Clinical Research Associate
- Site Monitoring Pro position located in Ontario, CA, United States.
The following role is for a Clinical Research Associate
- Site Monitoring Pro with IQVIA.
Our group is growing, and we are hiring a Clinical Research Associate
- Site Monitoring Pro in Ontario, CA, United States.
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