Clinical Research Associate

ICON

Los Angeles, CA, United States
Site visit and monitoring experience
Ich-gcp compliance
Clinical trial documentation management
Serve as the primary point of contact between investigational sites and the sponsor to ensure smooth clinical trial operations

Job Summary

  • Serve as the primary point of contact between investigational sites and the sponsor to ensure smooth clinical trial operations.
  • Maintain compliance with regulatory standards and manage detailed documentation in clinical trial management systems.
  • Collaborate with cross-functional partners and support site staff training to drive high-quality data and patient safety.

Matching Summary

Serve as the primary point of contact between investigational sites and the sponsor to ensure smooth clinical trial operations.

Skills & Requirements

Must-have

  • Site visit and monitoring experience
  • ICH-GCP compliance
  • Clinical trial documentation management
  • Patient safety monitoring and reporting
  • On-site monitoring in pharmaceutical or CRO industry
  • Drug accountability oversight
  • Cross-functional team collaboration

Nice-to-have

  • Clear communication skills
  • Problem-solving abilities
  • Collaborative team player
  • Experience with Oncology Hematology trials
  • Willingness to travel up to 50%

Key Requirements

  • Bachelor’s degree in Life Sciences or equivalent
  • Qualified Registered Nurse (RN)
  • 2+ years of on-site monitoring experience
  • Experience in Oncology Hematology clinical trials
  • 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