Sr. Cra

ICON Clinical Research, LP

East Coast, US
Fully remote
Ich gcp guidelines compliance
Site startup activities
Source document 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 plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.

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
  • site startup activities
  • source document verification
  • serious adverse event reporting
  • investigational product accountability

Nice-to-have

  • highly responsive and proactive
  • subject matter expert
  • leadership skills
  • team player

Key Requirements

  • 5+ years clinical monitoring experience
  • Oncology monitoring experience
  • feasibility/site selection/site start up experience
  • licensed health care professional
  • legally authorized to work in the United States

Work Rights

Not specified

Tailored Resume

Cover Letter