Cra Ii

ICON Clinical Research, LP

Romania
Fully remote
Conduct site visits
Ensure 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.
  • ICON plc is a world-leading healthcare intelligence and clinical research organization, proud to foster an inclusive environment driving innovation and excellence.
  • 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

  • Conduct site visits
  • Ensure protocol compliance
  • Data integrity and patient safety
  • Resolve data queries
  • Prepare study documentation

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Contribute to advancement of therapies
  • Nurture talent and reward performance

Key Requirements

  • Minimum 2 years CRA experience
  • Oncology experience preferred
  • In-depth knowledge of clinical trial processes
  • Familiarity with ICH-GCP guidelines
  • Ability to travel 60% of time
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter