Clinical Research Associate

ICON

Miami, FL, United States
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 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

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

Nice-to-have

  • Cross-therapeutic area experience
  • Immunology therapeutic area
  • Collaborative team player
  • Problem-solver

Key Requirements

  • 2+ years on-site monitoring experience
  • Bachelor's degree or RN
  • Eligible to work in US without sponsorship
  • Proficient in ICH-GCP
  • Travel up to 50%

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter