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#3081
Job Description:
- Overall responsibility for study management, responsible for the monitoring of studies in accordance with protocol/ SOPs/ Guidelines.
RESPONSIBILITIES:
- 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.

Skills:
molecular biology/ biochemistry/microbiology/ biotech/pharmacy/pharmacovigilance.

Experience: Fresher
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.
Salary: 15K-28K/M
Location: Pune

Click here & apply:-
https://www.exltech.in/clinical_researc ... 1cwJcEQMfo
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