Regulatory Medical Writer

1 week ago


London, Greater London, United Kingdom Life Sciences Recruitment Full time
Job Title: Regulatory Medical Writer

We are seeking skilled and experienced professionals to join our editorial team at Life Sciences Recruitment and contribute to the development of high-quality medical communications projects.

The role involves creating and delivering a broad array of medical communications projects, catering to the needs of pharmaceutical sponsors and healthcare professionals.

Responsibilities:
  • Develop high-quality written materials for assigned projects, including slide decks, email invitations, video scripts, advertisements, FAQ documents, case studies, and CPD modules.
  • Perform thorough copyediting and proofreading on a range of materials produced by other team members, ensuring coherence, structure, consistency, style, grammar/spelling accuracy, and alignment with the target audience.
  • Collaborate with design and digital teams to ensure creative concepts align with scientific messaging, and that all scientific claims and data are accurately represented.
  • Manage project materials for client review and approval using systems like Veeva Vault and ZincMaps, and efficiently manage these approval processes.
  • Make prioritization decisions to meet deadlines and project requirements.
  • Contribute to client services team discussions on suitable approaches for content development during project planning phases.
  • Format conference materials, including PowerPoint presentations, and conduct technical reviews to ensure optimal quality.

**Estimated Salary:** $80,000 - $110,000 per year

Requirements:
  • Bachelor's degree in life sciences, medicine, or a related technical discipline.
  • Minimum of 4 years' experience in a medical communications agency or pharmaceutical industry environment.
  • Strong understanding of core pharmacology principles, evidence-based medicine, and drug regulation/governance, including clinical trial types and the roles of regulatory bodies like NICE.
  • Excellent attention to detail, strong editing and proofreading skills, and a clear, direct writing style.
  • Familiarity with approval systems (e.g., Veeva Vault, ZincMaps) and a solid command of digital content management.


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