Clinical Site Manager Ii

ICON Clinical Research, LP

Paris, France
Overseeing clinical trial activities
Monitoring clinical trial sites
Ensuring data integrity
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence.
  • As a Senior CRA, 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 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

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

Skills & Requirements

Must-have

  • overseeing clinical trial activities
  • monitoring clinical trial sites
  • ensuring data integrity
  • participant safety
  • compliance throughout the study lifecycle
  • building effective relationships with site personnel

Nice-to-have

  • fostering an inclusive environment
  • driving innovation and excellence
  • shaping the future of clinical development
  • nurturing talent
  • work life balance opportunities

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
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter