Position: Executive
Experience: 2-7 Yrs
Qualification: M. Pharm (Pharmacology)

Job Responsibilities:
·      Feasibility assessment/ new product evaluation
·      Literature review and BA/BE study designing
·      BE Study Monitoring
·      Preparation of documents for regulatory submission (i.e BENOC, Import license application etc.)
·      Establishment and maintenance of study documents
·      Document preparation for dossier submission (i.e clinical overview, non-clinical overview, summery tables etc.)
·      Review of BE study documents i.e protocol, reports, ICF etc.
·      Preparation/review of medical write up
·      Coordination for serious adverse event reporting and safety update to Regulatory agency

Interested candidates can share their CVs on vilshashah@torrentpharma.com