Senior/Principal Medical Writer

📋 Description Lead preparation of complex regulatory docs. Collaborate with clinical teams and SMEs. Provide guidance to clients and project teams. Manage timelines, reviews, and deliverables. Coordinate with writers, QA, and support staff. Monitor budgets and ensure timely delivery. 🎯 Requirements Several years of clinical regulatory writing experience. Lead writer for multiple regulatory doc types. Senior: lead 3+ projects; Principal: lead 5+ projects. Experience with CTD dossiers and CTD types desirable. Direct client and cross-functional team interaction. Strong regulatory docs knowledge and tools. 🎁 Benefits Fully remote with Europe-wide flexibility. Contribute to meaningful regulatory programs. Competitive compensation by experience. Standard benefits and professional development. Work with experienced writers and international teams. High ownership across regulatory projects.