CRA II / Senior CRA
ICON · Buenos Aires, Argentina
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Role summary
This position involves overseeing clinical trial activities, including site visits, protocol compliance monitoring, and data quality assurance. The role requires a scientific or healthcare background and at least 1.5 years of clinical research experience, with demonstrated knowledge of GCP guidelines and trial regulations. Successful candidates will manage multiple deliverables while collaborating with site staff and investigators across study phases.
Privacy & handoff
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