Clinical Research Associate: On-site Monitoring & Site Management
Listed on 2026-10-06
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA is seeking an on-site Clinical Monitoring professional to ensure sites conduct studies per protocol, regulations, and sponsor requirements. You will monitor visits, track recruitment, and manage data queries while maintaining TMF/ISF documentation across US/Canada sites.
Ideal candidates have 2+ years of on-site monitoring experience, GCP/ICH familiarity, and strong English communication, organizational, and time-management skills.
This is a strong opening to take on the Clinical Research Associate:
On-site Monitoring & Site 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:
On-site Monitoring & Site Management role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
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