As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development as part of the Regulatory Affairs team
Job Summary
As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development as part of the Regulatory Affairs team.
You'll provide regulatory guidance and operational support across various stages of drug development, including early development, agency interactions, clinical trial applications, marketing applications, and post-approval staff.
In addition to your competitive salary, 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 Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development as part of the Regulatory Affairs team.
Skills & Requirements
Must-have
Regulatory guidance and operational support
Lead regulatory activities and submissions
CTA/IND/MAA experience
Participate in agency interactions
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Contribute to developing best practices
Key Requirements
Minimum of 6 years of experience
Bachelor's degree in scientific/healthcare field
Prior experience with various regulatory submissions