Senior Medical Writer | UK

TransPerfect·Remote jobRemotesenior

In short

→Redactar documentos clínicos y regulatorios de alta calidad para ensayos farmacéuticos.
→Dirigir equipos y tiempos de entrega en colaboración con áreas clínicas, reguladoras y operativas.
→Liderazgo en sistemas de gestión de documentos y procesos estructurados en entornos regulatorios.

Strong written and verbal communication skills in English

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The questions they'll ask you

1. ¿Cómo gestionarías un conflicto entre un revisor del cliente y un miembro del equipo durante una reunión de resolución de comentarios?

🔒 +7 more questions

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💵 USD · Remote · No visa

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What they ask for

✓5+ años como redactor médico en CRO/biotecnología/farmacéutica
✓Experiencia comprobada en redacción de informes de ensayos clínicos, protocolos e investigador brochures
✓Conocimiento de ICH y regulaciones estadounidenses y ex-US
✓Habilidades avanzadas en Microsoft Word y herramientas colaborativas
✓Capacidad de liderar reuniones de revisión y gestionar comentarios
✓Inglés fluido para comunicación escrita y verbal

Don't tick every box? That's normal — your free dossier shows your gaps and how to cover them in the interview.

Microsoft WordDocument Management SystemsCollaborative Authoring ToolsReview ToolsLean AuthoringStructured Content ManagementTemplatesStyle GuidesReference ManagementClient Document Systems

Who should you write to at TransPerfect?

Your free dossier identifies the people who'd interview you — their background, what they value, and how to reach out so you stand out before applying.

We’re seeking an organized, motivated, and collaborative individual for our medical writing team. The senior medical writer will partner cross-functionally with client teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management in leading the planning and preparation of high-quality clinical regulatory documents. The medical writer may produce protocols, publications, study reports, investigator brochures, narratives, and module documents, according to client and agency guidelines, to support drug development under brisk timelines. com .

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