Senior Medical Writer: Regulatory Documentation Lead

TransPerfect is seeking an organized, motivated senior medical writer to partner with Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management. You will lead planning and preparation of high-quality regulatory documents including protocols, publications, study reports, investigator brochures, narratives, and module documents within tight timelines. The role requires 5+ years of medical writing experience in CRO/biotech/pharmaceutical settings, a Bachelor's