Clinical Research Associate

ICON Clinical Research, LP

Miami, FL, 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, conducting all types of site visits

Job Summary

  • Serve as the primary point of contact between investigational sites and the sponsor, conducting all types of site visits.
  • Ensure site compliance with ICH-GCP, SOPs, and regulations, while maintaining up-to-date documentation in CTMS and eTMF systems.
  • ICON offers a range of benefits designed to be competitive 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, conducting all types of site visits.

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-functional collaboration
  • Problem-solving skills
  • Inclusive environment
  • Innovation and excellence

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
  • Experienced across multiple therapeutic areas
  • Proficient in ICH-GCP and clinical systems

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter