Senior Clinical Research Associate

ICON Clinical Research, LP

United States
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.
  • 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 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
  • ICH-GCP guidelines

Nice-to-have

  • foster an inclusive environment
  • nurtures talent
  • well-being and work life balance

Key Requirements

  • Minimum 1 year independent monitoring (CRA II)
  • Minimum 3 years independent monitoring (Senior CRA)
  • Bachelor's degree scientific/health-related field
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter