Senior Medical Writer | UK

TransPerfect·Remote jobRemotesenior

In short

→Escribe y dirige documentos clínicos reguladores de alto impacto para fármacos en entornos de desarrollo rápido.
→Coordinas equipos multidisciplinarios y herramientas digitales para cumplir plazos exigentes con calidad.
→Especialista en sistemas de gestión de documentos y enfoques estructurados, con experiencia clave en oncología e infecciosas.

Strong written and verbal communication skills in English

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The questions they'll ask you

1. ¿Cómo abordarías la coordinación de un informe de estudio clínico con múltiples revisores con feedback contradictorio?

🔒 +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 o farmacéutica
✓Experiencia comprobada en informes de estudios clínicos, protocolos y documentos de módulo 2/5
✓Dominio de ICH y regulaciones regulatorias (US y ex-US)
✓Capacidad para liderar reuniones de revisión y gestionar comentarios complejos
✓Habilidad probada en trabajo colaborativo con equipos de clínica, biostatística y regulación
✓Excelente comunicación escrita y oral en inglés

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

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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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