As a CRA at ICON, 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 CRA at ICON, 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 range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.
ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.
Matching Summary
As a CRA at ICON, 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
Regulatory compliance adherence
Good Clinical Practice (GCP) standards
Clinical trial software proficiency
Multi-site project management
Travel across Italy
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder relationship building
Problem-solving skills
Inclusive work environment
Key Requirements
Advanced degree in life sciences, nursing, or medicine