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1.0 - 2.0 years
1 - 2 Lacs
pune
Work from Office
Monitor and document all adverse events (AEs) and serious adverse events (SAEs) in accordance with study protocol, sponsor requirements, and applicable regulations. Ensure timely and accurate reporting of SAEs to the Ethics Committee, Sponsor, and Regulatory Authorities as required. Assist clinical staff in the identification, documentation, and classification of safety events. Maintain up-to-date safety tracking logs and ensure proper storage of safety documentation. Participate in safety review meetings and contribute to the preparation of safety summaries and reports. Liaise with investigators, data managers, and monitors to reconcile discrepancies related to safety data. Assist with trai...
Posted Date not available
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