Raman GN

I am holding a M.Sc. In Microbiology with 3 years of focused experience in regulatory writing, safety reports writing, client and vendor management.I have worked as a lead writer in different documents like CSRs, Clinical Overview, Clinical summary, DSURs, PBRERs, RMPS, patient narratives, CTRDs. Managed stakeholders from different line functions. A lead vendor coordinator and manage end to end process. Worked as a process trainer in TCS. I have experience in developing a wide range of scientific documents targeting the training, marketing, and awareness needs of various audiences from sales representatives, to physicians, to patients. Projects handled for various multinational and Indian pharma clients including Novartis, Roche, Novo Nordisk, Biocon etc. Have knowledge and ability to work on a wide range of therapeutic areas.