Clinical Research Associate

ICON Clinical Research, LP

Slovakia
Monitoring clinical trial sites
Ensure adherence to protocols
Gcp standards
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • monitoring clinical trial sites
  • ensure adherence to protocols
  • GCP standards
  • resolve site issues
  • timely data collection
  • site staff training

Nice-to-have

  • foster inclusive environment
  • drive innovation and excellence
  • advance innovative treatments
  • well-being and work life balance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • 3-6 years as Clinical Research Associate
  • Proven ability to manage multiple sites
  • Proficiency in clinical trial software
  • Ability to travel at least 60%
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter