Clinical Research Associate

ICON Clinical Research, LP

Seoul, South Korea
Fully remote
Clinical trial site monitoring
Adherence to study protocols
Gcp standards compliance
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.
  • As a Senior CRA, you will oversee and manage clinical trial activities, ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
  • ICON offers a competitive salary and a range of benefits designed for well-being and work-life balance, including various annual leave, health insurance, and retirement planning.

Matching Summary

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

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Adherence to study protocols
  • GCP standards compliance
  • Data integrity
  • Participant safety
  • Site performance assessment

Nice-to-have

  • Inclusive environment fostering innovation
  • Cross-functional team collaboration
  • Building effective relationships
  • Influencing and driving compliance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive Clinical Research Associate experience
  • Proven ability to manage multiple sites
  • Proficiency in clinical trial software
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter