Unblinded CRA
ICON · Warsaw, Poland
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Role summary
This Clinical Research Associate II role involves monitoring clinical trials, including site qualification, initiation, and close-out visits while ensuring protocol compliance and data integrity. The position requires a minimum of 2 years' CRA experience, a bachelor's degree in a scientific field, fluent German, and willingness to travel approximately 60%, with responsibilities spanning data review, investigator collaboration, and study documentation.
Privacy & handoff
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