0 - 2 years
13 - 16 Lacs
Posted:2 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities Clinical trial designing, protocol inputs for generic products and their FDCs The position is to Lead team of scientists to accomplish activities related to clinical trial designing, monitoring, concluding and MMA. Phase trials I IV execution. NDDS product development. Define objectives/ sample size calculation for protocols of clinical trials. AE/ SAE monitoring & reporting. Site selection/ site evaluation. Training to investigators, guide the trial site for execution of the study as per expectation of protocol. Preferred candidate profile Qualification : MD(Pharmacology) Interested candidates can share their CVs on vilshashah@torrentpharma.com
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