Clinical Site Associate (in-house Cra)

ICON Clinical Research, LP

Taipei, Taiwan
Site activation support
Essential document tracking
Clinical trial management systems
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.
  • You will work closely with Clinical Research Associates (CRAs), site staff, and cross-functional teams to help drive study start-up, maintenance, and close-out activities.
  • 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 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 support
  • essential document tracking
  • clinical trial management systems
  • site communication and follow-up
  • inspection and audit readiness

Nice-to-have

  • customer-focused approach
  • process improvement initiatives
  • foster an inclusive environment
  • nurtures talent

Key Requirements

  • Bachelor's degree or equivalent experience
  • Initial experience in clinical research
  • Strong organizational skills
  • High attention to detail
  • Effective written and verbal communication skills
  • Proficiency with MS Office
  • Ability to work collaboratively

Work Rights

Not specified

Tailored Resume

Cover Letter