Clinical Research Associate Ii

ICON

Utrecht, Netherlands
Fully remote
Clinical trial monitoring phase i–iii
Compliance with ich-gcp and regulations
Remote work with national travel
ICON plc is a global healthcare intelligence and clinical research organization committed to driving innovation, excellence, and inclusion

Job Summary

  • ICON plc is a global healthcare intelligence and clinical research organization committed to driving innovation, excellence, and inclusion.
  • This role involves independently monitoring Phase I–III clinical trials for small and medium sized biotech sponsors in the Netherlands, ensuring compliance and high-quality data.
  • ICON offers comprehensive CRA development programs and a range of competitive benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a global healthcare intelligence and clinical research organization committed to driving innovation, excellence, and inclusion.

Skills & Requirements

Must-have

  • Clinical trial monitoring Phase I–III
  • Compliance with ICH-GCP and regulations
  • Remote work with national travel
  • Fluency in Dutch and English
  • Valid driver’s license required

Nice-to-have

  • Collaboration with cross-functional teams
  • Problem-solving and organizational skills
  • Experience in biotech clinical trials
  • Structured CRA development programs

Key Requirements

  • Life science degree or equivalent
  • Minimum 2 years CRA experience
  • Knowledge of clinical trial processes and regulatory standards
  • Fluency in Dutch and English both spoken and written
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter