Posted:4 days ago| Platform:
On-site
Monitor clinical trial sites to ensure compliance with study protocols, GCP, and regulatory requirements. Perform site initiation, routine monitoring, and close-out visits. Assist in the preparation of regulatory submissions and documentation. Provide training and support to site staff as needed. Review and verify case report forms (CRFs) against source documents. Identify and resolve data discrepancies. Ensure proper documentation and timely reporting of adverse events. Job Types: Permanent, Fresher Pay: ₹25,001.03 - ₹40,100.97 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person
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