Sr. Cra

ICON plc

East Coast, US
Fully remote
Ich gcp guidelines compliance
Investigative site assessment
Clinical trial data verification
Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines

Job Summary

  • Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines.

Skills & Requirements

Must-have

  • ICH GCP guidelines compliance
  • Investigative site assessment
  • Clinical trial data verification
  • Serious adverse event reporting
  • Oncology monitoring experience

Nice-to-have

  • Highly responsive and proactive
  • Team player
  • Subject matter expert
  • Leadership skills

Key Requirements

  • 5+ years clinical monitoring experience
  • Undergraduate degree or equivalent
  • Licensed healthcare professional
  • Legal authorization to work in the US

Work Rights

Legally authorized to work in the United States

Tailored Resume

Cover Letter