- Support current product ideation, scientific feasibility assessment, and comparative evaluation of molecules / indications / platforms from a medical perspective
- Provide medical and scientific inputs to Business Development & Licensing activities, including:
- Scientific assessment of in‑licensing, co‑development, and partnership opportunities
- Evaluation of clinical data packages/data rooms, development status, unmet medical need, and differentiation.
- Support medical due diligence for BD transactions by reviewing:
- Conduct primary research through connects with medical fraternity to identify need gaps
- Clinical trial data (Phase I-IV)
- Safety, efficacy, and benefit-risk profiles
- Development plans,
regulatory pathways, and lifecycle potential.
- Prepare medical evaluation summaries and risk assessments for internal BD committees and senior management decision‑making.
- Work closely with BD, Regulatory Affairs, and Clinical teams to support go/no‑go decisions and portfolio prioritization.
- Review artworks and labels of all in-licensed products
Work Experience : 12+Years experience in a Pharmaceutical company