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. Lead the execution of documents, including project management tasks such as creating, maintaining, and communicating timelines quality control [QC], publishing) to ensure timely completion of documents Interpret data and create shell documents to support authoring Experience (5+ years)



as a medical writer in the CRO/biotech/pharmaceutical field Bachelor's degree or higher in a relevant field Familiarity with lean authoring approaches and structured content management Expertise with Microsoft Word and other Microsoft applications Service-oriented and proactive approach to project management Strong written and verbal communication skills in English TransPerfect provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law

📌 Senior Medical Writer | Spain (Lérida)
🏢 Transperfect
📍 Lérida