Clinical Site Associate

ICON Clinical Research, LP

United States Of America, United States
Site compliance
Accurate documentation
Audit and inspection readiness
ICON is currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team

Job Summary

  • ICON is currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team.
  • In this role, you will play a pivotal part in supporting clinical trial operations by ensuring site compliance, maintaining accurate documentation, and supporting audit and inspection readiness.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.

Matching Summary

ICON is currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team.

Skills & Requirements

Must-have

  • site compliance
  • accurate documentation
  • audit and inspection readiness
  • site-level communications
  • Trial Master File (TMF) maintenance

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • work life balance opportunities
  • diverse culture

Key Requirements

  • minimum of one year of experience as a Study Coordinator
  • Bachelor’s degree in Life Sciences or Healthcare
  • Previous experience in clinical research preferred

Work Rights

Not specified

Tailored Resume

Cover Letter