Assist in monitoring clinical trial sites to ensure adherence to study protocols SOPs and regulatory guidelines Support in reviewing essential clinical trial documents such as informed consent forms case report forms CRFs and investigator site files Participate in site initiation routine monitoring and close-out visits under supervision Ensure accurate and timely data collection entry and reporting Assist in identifying resolving and documenting protocol deviations and data discrepancies Maintain effective communication with investigators site staff and project teams Support the preparation of trial-related reports and regulatory submissions Ensure trial-related documentation is complete and up to date Job Types Full time Permanent Fresher Pay 226 488 77 - 538 976 46 per year Benefits Health insurance Paid sick time Work Location In person
📌 Clinical Research Associate (Karnataka)
🏢 Clariwell Global
📍 Karnataka
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