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.
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.
At ICON, inclusion & belonging are fundamental to our culture and values, and the company is committed to providing a workplace free of discrimination and harassment.
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 submissions CTA/IND/MAA
Lead regulatory activities independently
Provide regulatory guidance
Strong understanding of global regulatory requirements
Participate in agency interactions
Nice-to-have
Work collaboratively in cross-functional teams
Contribute to best practices development
Experience in pharmaceutical or biotechnology industry
Key Requirements
Bachelor's degree in scientific or healthcare-related field