Senior/Principal Medical Writer

📋 Description Lead preparation of complex clinical/regulatory docs Collaborate with clinical teams and stakeholders Provide document-specific guidance to clients Manage timelines, reviews, and deliverables Coordinate contributions from writers and QC Monitor budgets and ensure regulatory compliance 🎯 Requirements Several years writing clinical regulatory documents Lead writer for multiple regulatory types (≥3) Senior: lead >3 projects; Principal: lead >5 projects Experience with CTD dossiers and client-facing work Strong written/spoken English and attention to detail Interpersonal and communication skills; team collaboration 🎁 Benefits Fully remote with flexibility within Europe Contribute to meaningful clinical programs Competitive compensation based on experience Standard benefits and professional development Work with experienced professionals and international teams High ownership across regulatory projects