Conduct site qualification, initiation, monitoring, and close-out visits
Ensure protocol compliance, data integrity, and 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 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 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
Ensure protocol compliance, data integrity, and patient safety
Collaborate with investigators and site staff
Perform data review and resolution of queries
Contribute to study documentation preparation
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Advance innovative treatments and therapies
Nurture talent and reward high performance
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