As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Job Summary
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Key responsibilities include monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) 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.
Matching Summary
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Skills & Requirements
Must-have
Clinical trial monitoring
GCP standards adherence
Site performance assessment
Data collection and reporting
Cross-functional team collaboration
Stakeholder relationship management
Nice-to-have
Foster inclusive environment
Drive innovation and excellence
Continuous improvement focus
Guide other CRAs
Key Requirements
Bachelor's degree in relevant discipline
Extensive experience as a Clinical Research Associate