Senior Cra

ICON

Utrecht, Netherlands
Fully remote
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and compliance
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.
  • ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and the company is dedicated to providing an inclusive and accessible environment for all candidates.

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

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Data integrity and compliance
  • Site management and issue resolution
  • Cross-functional team collaboration
  • Ability to travel internationally and domestically

Nice-to-have

  • Training and guidance to site staff
  • Building effective stakeholder relationships
  • Fluency in Dutch and English
  • Strong organizational and problem-solving skills
  • Excellent communication and interpersonal skills

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive CRA experience with clinical trial knowledge
  • Valid driver’s license
  • Ability to travel at least 60% of the time
  • Fluency in Dutch and English

Work Rights

Not specified

Tailored Resume

Cover Letter