Principal Medical Writer - Oncology

As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Researches, writes, and edits clinical and regulatory documents by applying functional expertise and clinical drug development knowledge. Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents. Demonstrates technical expertise and background in the use of medical writing templates and software. Manages all aspects of the medical writing function. Contributes to clinical protocol development for first-in-human oncology studies. Drive the document preparation process, receive and review primary statistical output, draft and distribute documents for review, and incorporate/resolve comments with all reviewers. Provides scientific and medical writing consultancy to project teams, as requested.