As a CRA at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Job Summary
As a CRA at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Our biotech division of 8,000 people operates with a mindset aligned to small and mid-sized biopharma.
In addition to your competitive salary, 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 at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Skills & Requirements
Must-have
Monitoring clinical trial sites
Conducting site visits
Collaborating with cross-functional teams
Providing training and guidance
Building and maintaining relationships
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Tailored teams and management
Work life balance opportunities
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Certification (Italian Law)
Extensive experience as a Clinical Research Associate