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.
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USD/year
The Scientific Associate is responsible for developing and writing medical content for their assigned account(s). The SA works with internal teams to ensure the client vision is achieved and content is medically accurate. They are responsible for development of clinical monographs, value proposition slide decks, advisory board materials, and internal training resources. The role involves conducting literature reviews, refining content, and attending meetings.