Cra1/ii

ICON Clinical Research, LP

Utrecht, Netherlands
Hybrid
Monitoring clinical trial sites
Adherence to study protocols
Regulatory requirements and gcp
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
  • As a CRA, you will play a critical role in overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards.
  • ICON offers a competitive salary and a range of benefits designed for well-being and work-life balance, including health insurance, retirement planning, and employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.

Skills & Requirements

Must-have

  • monitoring clinical trial sites
  • adherence to study protocols
  • regulatory requirements and GCP
  • site performance assessment
  • data integrity and participant safety
  • cross-functional team collaboration

Nice-to-have

  • fostering an inclusive environment
  • driving innovation and excellence
  • shaping the future of clinical development
  • building effective relationships
  • influencing and driving compliance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Experience as a Clinical Research Associate
  • Strong understanding of clinical trial processes
  • Proven ability to manage multiple sites
  • Proficiency in clinical trial software
  • Ability to travel at least 60% of the time
  • Possess a valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter