Clinical Research Associate Ii/senior Cra

ICON

Warsaw, Poland
Fully remote
Clinical trial site visits
Protocol compliance monitoring
Data integrity assurance
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 benefits focused on well-being and work life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is committed to fostering an inclusive and accessible environment, providing equal employment opportunities without discrimination and offering reasonable accommodations for applicants with disabilities.

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

  • Clinical trial site visits
  • Protocol compliance monitoring
  • Data integrity assurance
  • Patient safety oversight
  • Collaboration with site staff
  • Travel up to 60%
  • Valid driver’s license

Nice-to-have

  • Strong organizational skills
  • Effective communication skills
  • Ability to work independently
  • Team collaboration in fast-paced environment

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years CRA experience
  • Knowledge of ICH-GCP guidelines
  • Valid driver’s license
  • Ability to travel internationally and domestically

Work Rights

Not specified

Tailored Resume

Cover Letter