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TransPerfect is seeking a senior medical writer to lead the planning and preparation of high-quality clinical regulatory documents, partnering with Clinical Development, Regulatory, Biostatistics, and Program Management to support drug development on tight timelines. You will produce protocols, publications, study reports, investigator brochures, narratives, and module documents, ensure adherence to client and agency guidelines, and drive document management and review processes across teams.

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Level

Senior L5

Location

New York, NY

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

today

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