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.
You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
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
clinical trial monitoring
protocol adherence
regulatory compliance
GCP standards
data integrity
participant safety
Nice-to-have
foster an inclusive environment
drive innovation and excellence
shape the 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