Clinical Site Manager Ii

ICON Broadbean

Warsaw, Poland
Clinical trial site monitoring
Adherence to study protocols
Regulatory requirements and gcp
ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.
  • As a Senior CRA, you will play a critical role in overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards.
  • ICON offers a competitive salary and a range of additional benefits designed to be competitive within each country, focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Adherence to study protocols
  • Regulatory requirements and GCP
  • Data integrity and participant safety
  • Site performance assessment
  • Effective stakeholder relationships

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Shaping the future of clinical development
  • Nurturing talent and rewarding performance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites and projects
  • Proficiency in relevant clinical trial software
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter