Position: Assistant Manager
Experience: 10-15 Years
Qualification: M. Pharm (Pharmacology)

Job Responsibilities:
·        Literature review and proposing possible clinical trial strategy.
·        Preparation of clinical trial synopsis.
·        Reviewing the clinical trial documents as protocol, IB, ICF etc.
·        Review study proposals and study plans received from CRO.
·        Study data monitoring for gaps, correctness on an ongoing basis.
·        Review of TLF’s and CSR.
·        Contribute in preparation of presentations for CT-NOC and MMA.
·        Constant literature reviews to provide updates to team on ongoing and projects in discussion.
·        Contribute in new product evaluation by preparing rationale, unmet need and proposing possible clinical strategy and study design.
·        Literature review for preparation of medical rationale, justifications and clinical trial waivers.
·        Contributing to create new product pipeline by continuously identifying new product and their presentation.
·        Contributing to create new NDDS product pipeline by continuously identifying new NDDS product and their presentation to team.

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