Principal/Head of Medical Writing

16 ore fa

Remote, Italia Experteer Italy Tempo pieno

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
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