1) To conduct primary and secondary research in pharmaceutical Industry for obtaining key qualitative and quantitative insights about various segments of the industry2) To collate the information from primary and secondary research to develop insights about the market and to forecast the trends for near future3) Highly engaged with rare consultations in pharmaceutical field which involves forecasting, competitive intelligence, and market analysis

1) To execute off-shore, ad-hoc, business research, and business development projects right from project scoping to preliminary research, effort estimation, conceptualization, methodology designing, conducting secondary research2) Secondary research involving data collection, data refining, data analysis, generating key insights, and providing strategic actionable intelligence to the client3) Client management by continuously communicating proceedings of the project and handling client queries4) Co-ordinate between the teams and ensure timely project delivery without compromising the quality of the deliverable5) Project Streamlining and Process Development6) Worked upon diverse projects in • Market Analysis • Medical Writing and Promotional Writing • Media Monitoring

1) Gained hands on experience in preparation of a diverse range of regulatory documents for filing of generic drugs, to worldwide regulatory bodies like US FDA, EMEA & MHRA, TGA, DCGI & several third world countries in Asia and Africa2) Regulatory Documents Prepared:• Prescribing Information; Summary of Product Characteristics and Patient Information Leaflet • Clinical & Non Clinical Overviews (Common Technical Documents)• Drafted a Clinical Expert Report• Systematic literature evaluation for additional safety filing of drugs to US FDA3) Acquired experience in drafting clinical trial documents like IB, ICD, Protocol, and CRF. 4) Got deep insights in designing a study, drafting and reviewing a study Protocol5) Got exposure to Pharmacovigilance processes, guidelines and practices