CRA II
ICON · Athens, Greece
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Role summary
This role involves managing clinical trial operations across sites in Greece, including qualification, monitoring, and closeout activities. The successful candidate will ensure protocol compliance, maintain data integrity, and collaborate with site staff while supporting trial documentation. A minimum of two years as a Clinical Research Associate is required, along with strong knowledge of clinical trial regulations and ICH-GCP guidelines; approximately 60% travel is necessary.
Privacy & handoff
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