Clinical Site Associate (in-house Cra)

ICON

Taipei, Taiwan
Clinical trial management systems
Site activation and document tracking
Site communication and query resolution
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 benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
  • At ICON, inclusion and belonging are fundamental to the culture and values, with a commitment 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

  • Clinical trial management systems
  • Site activation and document tracking
  • Site communication and query resolution
  • Logistics coordination for site visits
  • Essential document filing and maintenance
  • Collaborative team environment

Nice-to-have

  • Process improvement initiatives
  • Customer-focused site support
  • Adaptability to changing priorities
  • Proficiency with MS Office

Key Requirements

  • Bachelor’s degree or equivalent experience
  • Initial experience in clinical research or regulated environment
  • Effective written and verbal communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter