Clinical Research Associate Ii

ICON Clinical Research, LP

Czech Republic
Conducting site visits
Ensuring protocol compliance
Data integrity and patient safety
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.
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • 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.

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

  • Conducting site visits
  • Ensuring protocol compliance
  • Data integrity and patient safety
  • Collaborating with investigators
  • Performing data review
  • ICH-GCP guidelines

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Advancement of innovative treatments
  • Well-being and work life balance

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years experience as CRA
  • Ability to travel at least 60%
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter