S.NO Job Title Qualification Job Profile Apply
1.) Clinical Research Associate Pharma Professional who has sound knowledge of Clinical Trial Site Monitoring Creation & Development of Essential Clinical Trial Documents, Clinical Trial Site Selection, Monitoring. Apply
2.) Executive-DRA B.Pharm with diploma/ certificate in DRA M.Pharm(Pharmaceutics) 2 year Experience should be in Development of CTD and ACTD Development Regulatory Documentation,Preparing Dossiers, Review and Filling of Dossiers,Registration in Semi regulated and Regulated Markets and Dossiers preparation for non regulated markets. Apply
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