Torrent Pharma, the flagship Company of Torrent Group is one of the leading pharma companies of the Country. The Company was a pioneer in initiating the concept of niche marketing in India and today is ranked amongst the leaders in therapeutic segment of cardiovascular (CV), central nervous system (CNS), gastro-intestinal (GI) and women healthcare (WHC). The Company also has significant presence in diabetology, pain management, gynaecology, oncology and anti-infective segments. Torrent Pharma’s competitive advantage stems from the world-class manufacturing facilities, advanced R & D capabilities, extensive domestic network and a widespread global presence in over 40 countries.
Vacancy Details
Job description:
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 may share their CVs on vilshashah@torrentpharma.com
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