Ensure data integrity, participant safety, and compliance
Monitoring clinical trial sites
As a CRA at ICON Plc, 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 Plc, 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.
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 CRA at ICON Plc, 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
overseeing and managing clinical trial activities
ensure data integrity, participant safety, and compliance
monitoring clinical trial sites
conducting site visits
collaborating with cross-functional teams
building and maintaining effective relationships
Nice-to-have
foster an inclusive environment
driving innovation and excellence
diverse and dynamic team
well-being and work life balance
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites and projects
Proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills