Site qualification, initiation, monitoring, close-out
Protocol compliance, data integrity, patient safety
Data review and resolution of queries
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
site qualification, initiation, monitoring, close-out
protocol compliance, data integrity, patient safety
data review and resolution of queries
preparation and review of study documentation
Nice-to-have
foster an inclusive environment
drive innovation and excellence
advance innovative treatments and therapies
work life balance opportunities
Key Requirements
Bachelor's degree in scientific or healthcare field