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.
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.
At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.
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
study documentation preparation
ICH-GCP guidelines knowledge
Nice-to-have
inclusive environment
innovation and excellence
work life balance opportunities
diverse culture
Key Requirements
Minimum 1 year independent monitoring (CRA II)
Minimum 3 years independent monitoring (Senior CRA)