Theseniormedical writer will partner cross-functionallywith client teams inClinical Development, Clinical Operations,Biostatistics,Regulatory, and Program Management inleading theplanning and preparation of high-quality clinical regulatory documents. The medical writer may produceprotocols, publications, study reports, investigator brochures,narratives,and module documents, according to clientand agency guidelines,to support drug development underbrisktimelines.
quality control [QC], publishing)to ensuretimelycompletion ofdocuments
Interpret data and create shell documents to supportauthoring
Perform peer QC review asneeded
Contribute to medical writing operational initiatives (e.g., Experience (5+ years) as a medical writer in the CRO/biotech/pharmaceutical field




Bachelor's degreeor higherin a relevant field
Familiarity with lean authoring approachesand structured content management
Expertisewith Microsoft Word and other Microsoft applications
Strong written and verbal communication skillsin 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 (España)
🏢 Transperfect
📍 España