Study Start Up Associate

ICON Clinical Research, LP

Seoul, South Korea
Regulatory document preparation
Ethics committee submissions
Stakeholder coordination
As a Study Start Up Associate I/II/Sr. at ICON, you will play a pivotal role in leading 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/II/Sr. at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
  • Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
  • 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 Study Start Up Associate I/II/Sr. at ICON, you will play a pivotal role in leading 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
  • ethics committee submissions
  • stakeholder coordination
  • record maintenance
  • ICH-GCP compliance

Nice-to-have

  • process improvement initiatives
  • foster an inclusive environment
  • nurtures talent
  • work life balance opportunities

Key Requirements

  • minimum 1 year experience
  • life sciences degree
  • study start-up experience
  • local regulatory requirements knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter