Senior Cra

ICON Clinical Research, LP

Paris, France
Monitor clinical trial sites
Ensure adherence to protocols
Conduct site visits
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 adherence to protocols
  • Conduct site visits
  • Data integrity and site management
  • Proficiency in clinical trial software

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Shape the future of clinical development
  • Well-being and work life balance

Key Requirements

  • Extensive experience as a Clinical Research Associate
  • Strong understanding of clinical trial processes
  • Proven ability to manage multiple sites
  • Ability to travel at least 60% of the time
  • Possess a valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter