Associate Director, Global Scientific Communications, Medical Affairs

Role: Associate Director, Global Scientific Communications within Medical Affairs, remotely based, responsible for developing and managing scientific content supporting biopharma assets. Responsibilities: create high-quality materials (slide decks, narratives, FAQs) translating complex data into clear, compliant communications; support publication planning and execution; foster digital and innovative communication strategies; collaborate cross-functionally with Clinical, Regulatory, and Commercial teams; manage projects, timelines, and vendor relationships ensuring regulatory and SOP compliance. Requirements: advanced life sciences degree (PhD, PharmD, MD, or MS); 5+ years in medical/scientific content development within biotech/pharma; strong understanding of medical affairs, regulatory standards (FDA/EMA), and content management systems (e.g., Veeva); excellent writing, editing, project management, and cross-functional coordination skills. High-Value: experience in biotech/pharma medical communications, familiarity with digital engagement, and working in matrixed environments. Work setup: remote.