Clinical Research Associate Ii

ICON

Multiple Locations, TX, US
On-site monitoring experience
Ich-gcp compliance
Clinical trial management systems
Serve as the primary point of contact between investigational sites and the sponsor and conduct all types of site visits including selection, initiation, routine monitoring, and close-out

Job Summary

  • Serve as the primary point of contact between investigational sites and the sponsor and conduct all types of site visits including selection, initiation, routine monitoring, and close-out.
  • ICON offers a diverse culture that rewards high performance and nurtures talent with competitive salary and a range of benefits focused on well-being and work-life balance.
  • The company is committed to providing an inclusive and accessible environment and ensures equal employment opportunities without discrimination or harassment.

Matching Summary

Serve as the primary point of contact between investigational sites and the sponsor and conduct all types of site visits including selection, initiation, routine monitoring, and close-out.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • ICH-GCP compliance
  • Clinical trial management systems
  • Oncology clinical research
  • Patient safety monitoring
  • Site visit coordination
  • Drug accountability oversight

Nice-to-have

  • Collaborative team player
  • Problem-solving skills
  • Clear communication
  • Willingness to travel
  • Experience with hematology trials

Key Requirements

  • Bachelor’s degree in Life Sciences or equivalent
  • Qualified RN
  • 2+ years on-site monitoring experience
  • Experience in oncology clinical trials
  • Eligible to work in United States without visa sponsorship

Work Rights

Eligible to work in United States without visa sponsorship

Tailored Resume

Cover Letter