As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies
Job Summary
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
clinical trial monitoring experience
protocol compliance
data integrity
patient safety
site qualification
site initiation
site monitoring
site close-out visits
Nice-to-have
foster an inclusive environment
driving innovation and excellence
advancement of innovative treatments
collaborative work environment
work life balance opportunities
Key Requirements
Minimum of 2 years of experience
Bachelor's degree in scientific or healthcare field