Clinical Research Associate Ii / Senior Clinical Research Associate Large Pharma
ICON
Mechelen, Belgium
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and site management
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.
ICON offers a diverse culture that rewards high performance and nurtures talent with benefits focused on well-being and work-life balance for you and your family.
ICON is committed to providing an inclusive and accessible environment for all candidates and a workplace free of discrimination and harassment.
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 site monitoring
Good Clinical Practice (GCP) standards
Data integrity and site management
Cross-functional team collaboration
International and domestic travel
Valid driver’s license
Nice-to-have
Training and guidance to site staff
Stakeholder relationship management
Problem-solving skills
Organizational skills
Inclusive work environment
Key Requirements
Advanced degree in life sciences, nursing, or medicine