Senior Medical Writer — Remote Spain (Lead Clinical Docs)

Precision Medicine Group

Madrid

A distancia

EUR 60.000 - 90.000

Jornada completa

hace 1 hora
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Descripción de la vacante

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead development of clinical study documents for global programs. Remote in Spain, candidate will plan, write, edit, format, and QC documents in accordance with regulatory guidelines and company style.

The role requires 5+ years of senior medical writing experience, strong communication, meticulous attention to detail, and ability to work with sponsors, CROs, and internal teams to deliver high-quality

Formación

  • BS degree or equivalent in a scientific or medical discipline with relevant writing expertise.
  • 5+ years of experience as a Sr. Medical Writer in the sponsor and/or CRO setting or 7+ years of experience as a Principal Medical Writer.

Responsabilidades

  • Plan, write, edit, format, and QC clinical documents (protocols, IBs, CSRs, narratives) per regulatory guidance and eCTD requirements.
  • Manage documents from template to final approved versions with internal teams and external vendors.
  • Independently formulate key messages from clinical study data.
  • Draft complex content with strong writing and regulatory understanding.
  • Communicate clearly with internal and client teams, in writing and verbally.
  • Contribute to development of medical writing processes, SOPs, templates, and work instructions.

Conocimientos

Strong writing skills
Attention to detail
Communication skills
Independent working

Educación

BS degree or equivalent in scientific/medical discipline
MS/PhD preferred

Herramientas

Microsoft Windows
Teams
Word
Excel
Adobe Acrobat
PowerPoint

Descripción del empleo

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead development of clinical study documents for global programs. Remote in Spain, candidate will plan, write, edit, format, and QC documents in accordance with regulatory guidelines and company style.

The role requires 5+ years of senior medical writing experience, strong communication, meticulous attention to detail, and ability to work with sponsors, CROs, and internal teams to deliver high-quality

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