Clinical Research Associate, Single Sponsor Dedicated In Poland

IQVIA

Poland
Base: 132.800,00 zł - 280.000,00 zł; bonus/equity:...
Fully remote
Site selection and initiation
Protocol and training administration
Quality and 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 a strong advocate of diversity and inclusion in the workplace, believing that a work environment that embraces diversity will give us a competitive advantage.
  • The potential base pay range for this role, when annualized, is 132.800,00 zł - 280.000,00 zł.

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 initiation
  • protocol and training administration
  • quality and integrity evaluation
  • regulatory submissions tracking
  • Good Clinical Practice (GCP)
  • ICH guidelines

Nice-to-have

  • diversity and inclusion advocate
  • respectful workplace culture
  • maximize personal potential

Key Requirements

  • Bachelors Degree in scientific discipline or health care
  • 1 year on-site monitoring clinical trials
  • Proficiency in Microsoft Word, Excel, PowerPoint
  • Written and verbal communication skills
  • Good command of Polish and English language

Work Rights

Not specified

Tailored Resume

Cover Letter