Conduct site qualification, initiation, monitoring, and close-out visits
Ensuring protocol compliance, data integrity, and patient safety
Collaborating 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, fostering 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.
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
Conduct site qualification, initiation, monitoring, and close-out visits
Ensuring protocol compliance, data integrity, and patient safety
Collaborating with investigators and site staff
Performing data review and resolution of queries
Contributing to study documentation preparation and review
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Advancement of innovative treatments and therapies
Well-being and work life balance opportunities
Key Requirements
Minimum of 2 years of experience as a Clinical Research Associate
Bachelor's degree in a scientific or healthcare-related field
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines