Clinical Research Associate – Site Monitoring
Listed on 2026-09-29
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Research/Development
Research Assistant/Associate, Clinical Research
IQVIA is seeking a Research Associate to join our UK clinical operations team. The role focuses on on-site monitoring across diverse sites, ensuring GCP/ICH compliance and high-quality data capture.
The ideal candidate has at least 18 months of independent on-site monitoring experience, a life science degree or equivalent, and a willingness to travel to sites across the UK. You will work with cross-functional teams to support study conduct and site management.
Join us at IQVIA LLC as our next Clinical Research Associate – Site Monitoring & UK Travel in England, United Kingdom.
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 & UK Travel role in the description above.
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