Clinical Research Associate

ICON Clinical Research, LP

Chicago, IL, United States
On-site monitoring experience
Ich-gcp compliance
Ctms and etmf systems
Serve as the primary point of contact between investigational sites and the sponsor

Job Summary

  • Serve as the primary point of contact between investigational sites and the sponsor.
  • Ensure site compliance with ICH-GCP, SOPs, and regulations.
  • ICON offers a range of additional benefits designed to be competitive and focused on well-being and work-life balance.

Matching Summary

Serve as the primary point of contact between investigational sites and the sponsor.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • ICH-GCP compliance
  • CTMS and eTMF systems
  • Patient safety monitoring
  • Drug accountability oversight

Nice-to-have

  • Cross-therapeutic area experience
  • Collaborative team player
  • Problem-solving skills

Key Requirements

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

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter