Cra 1, Iqvia Biotech

IQVIA Biotech

Multiple Locations
Base: $71,900.00 - $119,900.00; bonus/equity: not ...
On-site monitoring experience
Oncology solid tumor monitoring
Protocol compliance
The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities

Job Summary

  • The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.
  • You will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines.
  • Accurate and timely documentation is critical; the CRA I prepare detailed monitoring visit reports, follow‑up letters, and all required study documentation to ensure audit readiness and transparent oversight.

Matching Summary

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

Salary

Base: $71,900.00 - $119,900.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • on-site monitoring experience
  • oncology solid tumor monitoring
  • protocol compliance
  • GCP and ICH guidelines
  • site management activities
  • patient safety protection

Nice-to-have

  • agile, therapeutically aligned solutions
  • trusted partnerships
  • breakthrough treatments
  • productive team relationships

Key Requirements

  • minimum 6 months on-site monitoring
  • Bachelor’s degree required
  • 6 months –2 years relevant experience
  • Basic knowledge of clinical research regulations

Work Rights

Not specified

Tailored Resume

Cover Letter