Posted:3 months ago|
Platform:
Work from Office
Full Time
Role & 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 Preferred candidate profile M. Pharm (Pharmacology) with 2-8 Yrs of Relevant Experience Interested candidates can share their CVs on vilshashah@torrentpharma / meghamaheshwari@torrentpharma.com
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Gandhinagar, Ahmedabad
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Gandhinagar, Ahmedabad
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Bengaluru
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