Clinical Research Associate

ICON

New York, NY, United States
On-site clinical monitoring experience
Ich-gcp compliance expertise
Clinical trial management systems
Serve as the primary point of contact between investigational sites and the sponsor to ensure compliance and data quality

Job Summary

  • Serve as the primary point of contact between investigational sites and the sponsor to ensure compliance and data quality.
  • Conduct all types of site visits including selection, initiation, routine monitoring, and close-out while maintaining up-to-date documentation.
  • Collaborate with cross-functional partners and support patient recruitment, safety monitoring, and site budget tracking.

Matching Summary

Serve as the primary point of contact between investigational sites and the sponsor to ensure compliance and data quality.

Skills & Requirements

Must-have

  • On-site clinical monitoring experience
  • ICH-GCP compliance expertise
  • Clinical trial management systems
  • Patient safety and AE/SAE reporting
  • Site visit coordination and documentation
  • Drug accountability oversight
  • Cross-functional collaboration

Nice-to-have

  • Clear communication skills
  • Problem-solving abilities
  • Collaborative team player
  • Willingness to travel frequently

Key Requirements

  • Bachelor’s degree in Life Sciences or equivalent
  • Qualified Registered Nurse (RN)
  • 2+ years on-site monitoring experience
  • Experience in Oncology Hematology
  • Eligible to work in United States without visa sponsorship
  • Willingness to travel up to 50%

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter