CRA 2
ICON · Blue Bell
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Role summary
Clinical Research Associate II responsible for monitoring clinical trials, including site qualification, initiation, and closeout visits. The role requires ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators and managing study documentation. Candidates need a bachelor's degree in a science or healthcare field, minimum two years of CRA experience, ICH-GCP knowledge, and willingness to travel approximately 60%.
Privacy & handoff
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