Site qualification, initiation, monitoring, close-out
Protocol compliance, data integrity, patient safety
Collaborate with investigators and site staff
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
Collaborate with investigators and site staff
Data review and query resolution
Global SIT Phase I to III onsite monitoring
Nice-to-have
Inclusive environment driving innovation
Diverse and dynamic team
Well-being and work life balance
Key Requirements
Minimum of 2 years of Global SIT Phase I to III onsite monitoring CRA experience
Bachelor's degree in a scientific or healthcare-related field
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines