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0.0 - 5.0 years
7 - 10 Lacs
ahmedabad
Work from Office
Role & responsibilities Clinical Research Physician-CPMA Monitor and manage adverse events Maintain and manage medical confidential reports Ensure compliance to protocol and SOPs Adverse tracking and follow-up of subjects Coordinate with screening and volunteer recruitment group on updates regarding volunteers adverse events and follow-up Handle safety related issues prior to and during the clinical phase of the study. Coordinate and conduct staff vaccination program and other related activities Others: Support clinical trial group Help for corporate check-up Write and review related SOPs Help maintain and update all the systems and SOPs in the department Train the staff on all SOPs related ...
Posted 7 hours ago
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