A Senior Medical Writer job description includes
writing and editing complex clinical and regulatory documents, such as clinical study reports, investigator brochures, and regulatory submissions, while adhering to strict guidelines. Key responsibilities involve collaborating with cross-functional teams like scientists and statisticians, managing timelines and review processes, conducting literature reviews, and mentoring junior staff. The role requires strong analytical skills, deep knowledge of scientific and regulatory processes, and the ability to interpret and present complex data accurately and concisely

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