- Overall responsibility for study management, responsible for the monitoring of studies in accordance with protocol/ SOPs/ Guidelines.
- Track all adverse event reports received and completed Review and assess all source documents, and compile data in an adverse event report
- Code adverse events in the client safety database Release report to the client through the client safety database.
molecular biology/ biochemistry/microbiology/ biotech/pharmacy/pharmacovigilance.
Education :Msc., lifescience,nursing , B.Pharmacy/M.Pharmacy/ PharmD, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S, etc.) and lifescience graduates.
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https://www.exltech.in/clinical_researc ... 1cwJcEQMfo