Team: Clinical Reporting

Location : Bangalore, Novo Nordisk Global Business Services (GBS), India

Your New Role

As a Medical Writer, you will perform a wide range of medical writing tasks to support clinical development programs, delivering high-quality content and documents that align with the Clinical Reporting strategy. The tasks for trial and/or non-trial activities within clinical reporting will include but will not be limited to preparation of Protocols, Clinical Trial Reports (CTRs), Investigator Brochure (IB), CTD Module 2 summaries and overview (clinical submission documents) and Regulatory response documents (Q&A).

You will act as a primary contact for stakeholders on Clinical Reporting-driven content, drive discussions to ensure decisions align with strategy, and represent Clinical Reporting in relevant project groups.

Key responsibilities