Cra I

ICON

Paris, , France
Hybrid
On-site clinical trial monitoring
Compliance with ich-gcp standards
French regulatory knowledge
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • As a CRA I, you will support Phase II–IV clinical trials ensuring compliance with protocols, ICH-GCP, and French regulations while maintaining strong site partnerships.
  • ICON offers structured CRA development pathways, ongoing training, clear progression opportunities, and a range of benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • On-site clinical trial monitoring
  • Compliance with ICH-GCP standards
  • French regulatory knowledge
  • Source data verification
  • Hybrid work environment
  • Travel across France

Nice-to-have

  • Strong organizational skills
  • Excellent communication skills
  • Collaborative team environment
  • Fluency in French and English
  • Patient safety focus

Key Requirements

  • Degree in Life Sciences or related discipline
  • Minimum 12 months independent on-site monitoring experience
  • Fluency in French and English
  • Valid driver’s license
  • Experience with Phase II–IV studies preferred

Work Rights

Not specified

Tailored Resume

Cover Letter