Clinical Research Associate

ICON plc

Connecticut, United States
Base: $91,336.00-$114,170.00; bonus/equity: not sp...
On-site monitoring experience
Ich-gcp and regulations
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 competitive salary, a range of benefits including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

Serve as the primary point of contact between investigational sites and the sponsor, conducting all types of site visits.

Salary

Base: $91,336.00-$114,170.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

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

Nice-to-have

  • Collaborative team player
  • Clear communicator
  • Problem-solver
  • Fostering inclusive environment

Key Requirements

  • 2+ years on-site monitoring experience
  • Bachelor's degree or RN
  • Eligible to work in United States
  • Experience monitoring Oncology studies

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter