Principal Medical Writer

ICON Clinical Research, LP

Multiple Locations
Fully remote
Lead regulatory and clinical documents
Develop high-quality regulatory documents
Gather and synthesize information
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information

Job Summary

  • As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information.
  • ICON plc is a world-leading healthcare intelligence and clinical research organization, proud to foster an inclusive environment driving innovation and excellence.
  • 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 Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information.

Skills & Requirements

Must-have

  • lead regulatory and clinical documents
  • develop high-quality regulatory documents
  • gather and synthesize information
  • adherence to regulatory requirements

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • commitment to high standards

Key Requirements

  • Advanced degree in life sciences
  • Minimum 5 years experience
  • Significant experience in medical writing
  • Strong understanding of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter