Senior/principal Medical Writer

ICON Clinical Research, LP

UK
Fully remote
Author regulatory documents
Interpret and summarize data
Lead meetings and drive decisions
As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence

Job Summary

  • As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
  • Independently author most study-level documents at simple to complex levels, for example: Protocol, protocol outlines Subject Information/Informed Consent Clinical study reports (CSRs) Lay summaries of clinical trial results Investigator brochures (IBs).
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Skills & Requirements

Must-have

  • Author regulatory documents
  • Interpret and summarize data
  • Lead meetings and drive decisions
  • Manage medical writing projects
  • Stakeholder alignment and coordination

Nice-to-have

  • Pro-active team player
  • Build good working relationships
  • Strong engagement with stakeholders
  • Resourcefulness and independent work

Key Requirements

  • Experienced in writing regulatory documents
  • Submission experience
  • 1 year fixed term contract

Work Rights

Not specified

Tailored Resume

Cover Letter