(senior) Clinical Research Associate - Sponsor Dedicated
ICON Clinical Research, LP
Frankfurt, Germany
Gcp standards adherence
Clinical trial site monitoring
Data integrity and reporting
As a Senior 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 Senior 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.
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Matching Summary
As a Senior 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
GCP standards adherence
clinical trial site monitoring
data integrity and reporting
site performance assessment
stakeholder relationship management
Nice-to-have
fostering inclusive environment
driving innovation and excellence
shaping future of clinical development
work life balance opportunities
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate