Clinical Site Manager Ii

ICON

Warsaw, Poland
Monitoring clinical trial sites
Adherence to study protocols
Regulatory requirements and gcp
ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities.
  • Key responsibilities include monitoring sites for protocol adherence, conducting site visits, collaborating with teams for data collection, and training site staff.
  • ICON offers a competitive salary, diverse benefits focused on well-being and work-life balance, and is committed to an inclusive and accessible environment.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities.

Skills & Requirements

Must-have

  • Monitoring clinical trial sites
  • Adherence to study protocols
  • Regulatory requirements and GCP
  • Conducting site visits
  • Data integrity and participant safety
  • Collaboration with cross-functional teams

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Building effective relationships
  • Influencing and driving compliance

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 clinical trial software and tools
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter