TransPerfect seeks an organized, motivated senior medical writer to lead cross-functional planning and preparation of high-quality regulatory documents in Barcelona. You will collaborate with Clinical Development, Biostatistics, Regulatory, and Program Management to produce protocols, study reports, narratives, and investigator brochures under tight timelines.
The role requires 5+ years in medical writing within CRO/biotech/pharma, a Bachelor’s degree or higher, and experience with
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📌 Senior Medical Writer — Lead Regulatory Docs (Barcelona)
🏢 Transperfect
📍 Barcelona
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