Job Summary

• As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.
• Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity, and compliance with regulatory guidelines and industry standards.
• 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

Skills & Requirements

Key Requirements

• 3-5 years of experience in medical writing
• Advanced degree in Life Sciences, Pharmacy, Medicine
• Proficiency in interpreting complex clinical trial data
• Strong understanding of regulatory requirements
• Business level English proficiency

Work Rights