Regulatory Affairs Manager

ICON plc

South Korea
Fully remote
Regulatory submissions cta/ind/maa
Lead internal regulatory teams
Global regulatory requirements knowledge
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 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 internal regulatory teams
  • Global regulatory requirements knowledge
  • Regulatory guidance in drug development
  • Independent regulatory activity management

Nice-to-have

  • Collaborative cross-functional teamwork
  • Insight of regulatory processes and guidelines
  • Experience in pharmaceutical or biotechnology industry
  • Inclusive and diverse work environment

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum of 6 years regulatory affairs experience
  • Prior experience with CTA/IND/MAA submissions

Work Rights

Not specified

Tailored Resume

Cover Letter