Clinical Research Associate

ICON

Chicago, IL, United States
On-site monitoring experience
Ich-gcp compliance
Clinical trial documentation systems
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • The Clinical Research Associate will serve as the primary contact between investigational sites and sponsors, ensuring compliance and supporting site operations.
  • ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • on-site monitoring experience
  • ICH-GCP compliance
  • clinical trial documentation systems
  • site visit coordination
  • patient safety monitoring
  • drug accountability management

Nice-to-have

  • cross-functional collaboration
  • problem-solving skills
  • clear communication
  • team player
  • experience in multiple therapeutic areas

Key Requirements

  • Bachelor’s degree in Life Sciences or equivalent
  • Qualified RN
  • 2+ years on-site monitoring experience
  • Eligible to work in United States without visa sponsorship

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter