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Job description

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) with 03-04 Yrs relevant experience Interested candidates are requested to share their CVs on vilshashah@torrentpharma.com

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