Clinical Research Associate Ii / Senior Clinical Research Associate Large Pharma
ICON Clinical Research, LP
Mechelen, Belgium
Oversee and manage clinical trial activities
Ensure data integrity and participant safety
Conduct site visits and provide support
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.
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 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
Oversee and manage clinical trial activities
Ensure data integrity and participant safety
Conduct site visits and provide support
Monitor clinical trial sites
Adherence to study protocols and GCP
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Shape the future of clinical development
Build and maintain effective relationships
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