Clinical Research Associate

ICON

Missouri, US
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 role involves serving as the primary contact between investigational sites and sponsors, ensuring compliance, monitoring patient safety, and supporting recruitment efforts.
  • ICON offers a diverse culture with competitive salary, comprehensive benefits focused on well-being and work-life balance, and an inclusive workplace free from discrimination.

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
  • Patient safety monitoring
  • Site visit coordination
  • Drug accountability management

Nice-to-have

  • Collaborative team player
  • Problem-solving skills
  • Clear communication
  • Experience in multiple therapeutic areas
  • Willingness to travel up to 50%

Key Requirements

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

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter