Clinical Research Coordinator - Brno

IQVIA

Brno, Czech Republic
Fully remote
Maintain study documentation
Support patient screening and enrollment
Coordinate study procedures
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks

Job Summary

  • As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks.
  • The position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
  • At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science.

Matching Summary

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks.

Skills & Requirements

Must-have

  • Maintain study documentation
  • Support patient screening and enrollment
  • Coordinate study procedures
  • Perform data entry and quality checks
  • Communicate with study monitors
  • Proficiency in MS Office applications

Nice-to-have

  • Excellent interpersonal skills
  • Strong organizational skills
  • Attention to detail

Key Requirements

  • Bachelor’s degree in life sciences or equivalent
  • 1-2 years experience as CRC/CRA/RN
  • Fluency in Czech
  • Good command of English

Work Rights

Not specified

Tailored Resume

Cover Letter