Senior Cra

ICON Clinical Research, LP

Us
Fully remote
Protocol compliance
Data integrity
Patient safety
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.
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • In addition to your competitive salary, ICON offers a range of additional benefits. 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

  • protocol compliance
  • data integrity
  • patient safety
  • site qualification
  • site initiation
  • site monitoring
  • site close-out visits

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • advancement of innovative treatments
  • work life balance opportunities

Key Requirements

  • 1 year independent monitoring
  • 3 years independent monitoring
  • Bachelor's degree scientific or healthcare
  • ICH-GCP guidelines knowledge
  • travel at least 60%

Work Rights

Not specified

Tailored Resume

Cover Letter