Site Management Associate

ICON

Seoul, South Korea
Site monitoring activities
Study protocol adherence
Good clinical practice (gcp) guidelines
As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency

Job Summary

  • As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.
  • You will contribute to the success of clinical research by providing essential administrative and logistical support to site management teams.
  • 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 Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.

Skills & Requirements

Must-have

  • Site monitoring activities
  • Study protocol adherence
  • Good Clinical Practice (GCP) guidelines
  • Documentation preparation
  • Data entry
  • Tracking site performance metrics

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Collaborating with cross-functional teams
  • Enhancing knowledge and skills

Key Requirements

  • Bachelor’s degree in relevant field
  • 2+ years Global SIT IRB submission experience
  • Experience in clinical research or site management preferred

Work Rights

Not specified

Tailored Resume

Cover Letter