Clinical Research Associate

ICON plc

Miami, FL, United States
Ich-gcp compliance
Site monitoring visits
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 and maintain up-to-date documentation in CTMS and eTMF systems.
  • 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

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

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • site monitoring visits
  • CTMS and eTMF systems
  • patient safety monitoring
  • drug accountability oversight
  • cross-functional collaboration

Nice-to-have

  • inclusive environment
  • innovation and excellence
  • mission to shape the future
  • well-being and work life balance

Key Requirements

  • Bachelor’s degree in Life Sciences or equivalent, or qualified RN
  • 2+ years on-site monitoring experience
  • Eligible to work in United States without visa sponsorship
  • Experienced across multiple therapeutic areas
  • Proficient in ICH-GCP, local regulatory requirements
  • Willing and able to travel up to 50%

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter