Job description

Experience 1 - 10 years of experience in Medical Writing Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document Clinical Summary of Efficacy and Common Technical Document.

Skills Required

Key Skills

• CSR
• NARRATIVES
• MEDICAL WRITING
• IB
• CLINICAL DOCUMENTS

Other Information