Updated: Today
Location: Madrid, Spain
Job ID: -OTHLOC-3651-2DH

Medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory documents to ensure high-quality completion of all assigned writing projects.

Job Responsibilities

• Compiles, writes, edits, and coordinates medical writing deliverables, presenting scientific information clearly and accurately, and works as a medical writer within and across departments with moderate supervision.
• Completes a variety of documents including clinical study protocols and protocol amendments, clinical study reports, patient narratives, and investigator brochures.
• Adheres to established regulatory standards, including ICH E3 guidelines, company SOPs, client standards, approved templates, authorship requirements, and style and formatting guides, ensuring timely and budget‑constrained project delivery. ...