Assist in setting up monitoring and closing clinical trial sites Ensure that clinical trials are conducted according to protocol GCP ICH guidelines and local regulatory requirements Perform regular site visits if applicable to ensure compliance and data accuracy Support in the collection and review of essential documents Communicate with clinical trial sites sponsors and internal teams Assist in preparing study-related documentation and reports Maintain and track clinical trial supplies Job Types Full time Permanent Fresher Pay 22 743 24 - 35 294 44 per month Benefits Paid sick time Provident Fund Work Location In person
📌 Clinical Research Associate (Maharashtra)
🏢 Clariwell Global
📍 Maharashtra
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