Job Summary

• You will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.
• Key responsibilities include 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.
• 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.

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Skills & Requirements

Key Requirements

• Bachelor's degree in scientific discipline
• Proficiency in interpreting complex data
• Strong understanding of regulatory requirements
• Experience interacting with regulatory agencies
• Ability to manage multiple projects

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