Principal/Head Of Medical Writing

As a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape scientific communication and contribute to improving patient outcomes on a global scale.

• competitive salary package (GBP)
• on-site role
• Lead development and review of clinical and regulatory documents ensuring compliance with industry standards
• Manage multiple projects with timelines and deliverables across teams
• Build strong working relationships with clinical and regulatory personnel to streamline information flow
• Drive innovative approaches to scientific writing for clarity and impact
• Analyze and interpret complex data to produce concise documentation
• Maintain up-to-date knowledge of regulatory requirements and industry best practices
• Extensive experience in medical or scientific writing within the life sciences
• Proven ability to manage large, complex documentation projects
• Excellent understanding of regulatory guidelines and submission processes
• Strong communication skills and attention to detail
• Proficiency with relevant document management tools and software
• Relevant certifications or advanced degrees in life sciences are preferred
• Strong communication
• Cross-functional collaboration
• Document management tools and software

Principal/Head of Medical Writing • cagliari, sardegna, it