Clinical Research Associate 3

ICON Clinical Research, LP

Turkey
Monitoring clinical trial sites
Ensure adherence to study protocols
Good clinical practice (gcp) standards
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 plc is a world-leading healthcare intelligence and clinical research organization, proud to foster an inclusive environment driving innovation and excellence.
  • 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

  • monitoring clinical trial sites
  • ensure adherence to study protocols
  • Good Clinical Practice (GCP) standards
  • data integrity
  • participant safety
  • compliance throughout the study lifecycle

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • shape the future of clinical development
  • well-being and work life balance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • 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