Senior/principal Medical Writer

ICON

Multiple Locations, , UK/Europe
Fully remote
Regulatory document writing experience
Clinical study report authoring
Project management of medical writing
As a Senior Medical Writer you will be fully dedicated to a Top-5 pharmaceutical company while benefiting from ICON's learning opportunities and long-term career development

Job Summary

  • As a Senior Medical Writer you will be fully dedicated to a Top-5 pharmaceutical company while benefiting from ICON's learning opportunities and long-term career development.
  • You will independently author a variety of clinical research documents including protocols, clinical study reports, and informed consent forms, while leading meetings and driving decisions on medical writing issues.
  • ICON offers a diverse and inclusive culture with competitive salary and benefits focused on well-being and work-life balance for you and your family.

Matching Summary

As a Senior Medical Writer you will be fully dedicated to a Top-5 pharmaceutical company while benefiting from ICON's learning opportunities and long-term career development.

Skills & Requirements

Must-have

  • Regulatory document writing experience
  • Clinical study report authoring
  • Project management of medical writing
  • Stakeholder engagement and alignment
  • Independent medical writing capability

Nice-to-have

  • Pro-active team player
  • Strong facilitation and communication skills
  • Resourcefulness with SOPs and guidance
  • Experience with pharmaceutical or CRO clients

Key Requirements

  • Experience writing regulatory documents
  • Submission document experience
  • Project management of medical writing projects
  • Ability to work independently
  • UK or Europe home-based work eligibility

Work Rights

Not specified

Tailored Resume

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