Regulatory Affairs Associate

ICON plc

Seoul, South Korea
Fully remote
Regulatory document preparation
Clinical trial applications
Ethics committee submissions
As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
  • ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Regulatory document preparation
  • Clinical trial applications
  • Ethics committee submissions
  • Stakeholder coordination
  • Record maintenance

Nice-to-have

  • Life sciences degree
  • Collaboration with cross-functional teams
  • Independent work
  • Fast-paced environment

Key Requirements

  • Bachelor's degree in life sciences
  • Previous experience in clinical research
  • Previous experience in regulatory affairs
  • Home-based in South Korea

Work Rights

Not specified

Tailored Resume

Cover Letter