Clinical Trial Site Monitor
Listed on 2026-10-08
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Science
Clinical Research
IQVIA is seeking a site monitoring professional to ensure study conduct across multiple U.S. locations. You will perform visits, support subject recruitment, and train site staff in protocol requirements.
The role emphasizes GCP/ICH compliance, data integrity, and effective communication with investigators. A bachelor's degree and 2+ years of on-site monitoring are expected, with strong English skills and teamwork.
The following opening is for a Clinical Trial Site Monitor with IQVIA.
This is a strong position to take on the Clinical Trial Site Monitor role at IQVIA.
As a Clinical Trial Site Monitor, you will play an important part at IQVIA in Littleton, CO, United States.
We invite applications for the Clinical Trial Site Monitor position located in Littleton, CO, United States.
Our team is growing, and we are hiring a Clinical Trial Site Monitor in Littleton, CO, United States.
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