Senior Cra

ICON plc

Czech Republic
Conduct site qualification visits
Ensure protocol compliance
Maintain high-quality clinical data
As a Clinical Research Associate II 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 II 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.
  • 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.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Clinical Research Associate II 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

  • Conduct site qualification visits
  • Ensure protocol compliance
  • Maintain high-quality clinical data
  • ICH-GCP guidelines knowledge
  • Travel at least 60% of the time

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Contribute to advancement of therapies
  • Work life balance opportunities

Key Requirements

  • Minimum 2 years CRA experience
  • Bachelor's degree scientific/healthcare
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter