Senior Cra

ICON Clinical Research, LP

Los Angeles, California, USA
Overseeing and managing clinical trial activities
Ensure data integrity, participant safety
Monitoring clinical trial sites
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

Matching Summary

As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • overseeing and managing clinical trial activities
  • ensure data integrity, participant safety
  • monitoring clinical trial sites
  • adherence to study protocols
  • Good Clinical Practice (GCP) standards
  • clinical trial software and tools

Nice-to-have

  • advanced degree in life sciences
  • building and maintaining effective relationships
  • ability to influence and drive compliance

Key Requirements

  • Advanced degree in a relevant field
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites
  • Expertise in monitoring practices
  • Five years of CRA experience
  • phase I oncology monitoring experience
  • Ability to travel at least 60% of the time
  • valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter