Principal Medical Writer

ICON Clinical Research, LP

Paris, France
Fully remote
Lead medical writing document preparation
Develop regulatory and clinical documents
International regulatory guidance and requirements
We are currently seeking Senior or Principal Medical Writer to join our diverse and dynamic team

Job Summary

  • We are currently seeking Senior or Principal Medical Writer to join our diverse and dynamic team.
  • At this role you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information.
  • Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Matching Summary

We are currently seeking Senior or Principal Medical Writer to join our diverse and dynamic team.

Skills & Requirements

Must-have

  • lead medical writing document preparation
  • develop regulatory and clinical documents
  • international regulatory guidance and requirements
  • clinical development processes
  • ICH guidelines

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • well-developed oral and written communication
  • problem-solving and interpersonal skills

Key Requirements

  • Bachelor's degree in science
  • At least 5 years of experience
  • 3+ years of electronic documents and submissions
  • Experience as lead writer for key documents

Work Rights

Not specified

Tailored Resume

Cover Letter