Clinical Research Associate - Iqvia Biotech Poland

IQVIA

Warsaw, Poland
Base: 132.800,00 zł - 280.000,00 zł; bonus/equity:...
Fully remote
Site selection and management
Protocol adherence monitoring
Data integrity evaluation
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
  • IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
  • We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Matching Summary

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Salary

Base: 132.800,00 zł - 280.000,00 zł; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Site selection and management
  • Protocol adherence monitoring
  • Data integrity evaluation
  • Regulatory submission tracking
  • Subject recruitment planning

Nice-to-have

  • Patient outcome impact
  • Intelligent connections
  • Honesty and professionalism

Key Requirements

  • Bachelor's degree or educational equivalent
  • 2 years on-site monitoring experience
  • Proficiency in Polish and English

Work Rights

Not specified

Tailored Resume

Cover Letter