Clinical Research Associate

ICON plc

New York, NY, United States
On-site monitoring experience
Proficient in ich-gcp
Experience in oncology hematology
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.
  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting.

Matching Summary

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

Skills & Requirements

Must-have

  • On-site monitoring experience
  • Proficient in ICH-GCP
  • Experience in Oncology Hematology

Nice-to-have

  • Clear communicator
  • Collaborative team player
  • Problem-solving skills

Key Requirements

  • Bachelor’s degree in Life Sciences
  • 2+ years of clinical research experience
  • Eligible to work in the United States

Work Rights

Not specified

Tailored Resume

Cover Letter