Clinical Research Associate - Site Monitoring & Trial Delivery
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure protocol compliance and data integrity. The role requires coordinating with site staff, training personnel, and supervising regulatory submissions and data management activities.
Candidates should have at least two years of on-site monitoring experience, familiarity with GCP/ICH, and strong English communication skills. The position emphasizes collaboration with the study team and adherence to sponsor requirements.
The following opening is for a Clinical Research Associate
- Site Monitoring & Trial Delivery with 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
- Site Monitoring & Trial Delivery role in the description above.
We appreciate your interest in this position.
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