Senior Cra

ICON Clinical Research, LP

Utrecht, Netherlands
Fully remote
Monitor clinical trial sites
Ensure data integrity
Participant safety
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • monitor clinical trial sites
  • ensure data integrity
  • participant safety
  • compliance throughout study lifecycle
  • conduct site visits
  • provide training and guidance

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • shape the future of clinical development
  • well-being and work life balance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites
  • Proficiency in clinical trial software
  • Fluently in Dutch and English
  • Ability to travel at least 60% of the time

Work Rights

Not specified

Tailored Resume

Cover Letter