Principal Medical Writer

ICON Clinical Research, LP

Multiple Locations
Fully remote
Develop and execute medical writing strategies
Write clinical pharmacology documents
Summarize complex clinical trial data
As a Principal Medical Writer, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects

Job Summary

  • As a Principal Medical Writer, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects.
  • Deliver high quality relevant Clinical Pharmacology & Pharmacometrics (CPP) documents, as well as CSRs, protocols, and other documents, within the required regulatory system.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.

Matching Summary

As a Principal Medical Writer, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects.

Skills & Requirements

Must-have

  • Develop and execute medical writing strategies
  • Write clinical pharmacology documents
  • Summarize complex clinical trial data
  • Interpret statistical analyses
  • Adhere to regulatory requirements ICH-GCP

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Collaborate effectively with cross-functional teams
  • Build relationships with key stakeholders

Key Requirements

  • Advanced degree in Life Sciences, Pharmacy, Medicine
  • 3-5 years medical writing experience
  • Experience in Module 2.7.1 and 2.7.2
  • Proficiency in scientific writing and editing
  • Understanding of regulatory requirements FDA, EMA

Work Rights

Not specified

Tailored Resume

Cover Letter