Clinical Site Associate

ICON Clinical Research, LP

China
Site activation document collection
Clinical trial management systems
Site communication and follow-up
As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards

Job Summary

  • As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.

Skills & Requirements

Must-have

  • Site activation document collection
  • Clinical trial management systems
  • Site communication and follow-up
  • Essential document filing and maintenance
  • Timely site payment processing

Nice-to-have

  • Customer-focused approach
  • Process improvement initiatives
  • Sharing best practices
  • Inclusive and accessible environment

Key Requirements

  • Bachelor's degree or equivalent experience
  • Initial clinical research experience preferred
  • Proficiency with MS Office and electronic systems

Work Rights

Not specified

Tailored Resume

Cover Letter