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