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 range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
At ICON, inclusion & belonging are fundamental to our culture and values, and the company is committed to providing 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 compliance
Site performance assessment
Cross-functional team collaboration
Travel at least 60% internationally and domestically
Valid driver’s license
Nice-to-have
Training and guidance to site staff
Strong organizational and problem-solving skills
Excellent communication and interpersonal skills
Stakeholder management
Ability to influence compliance
Experience with clinical trial software and tools
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Ability to manage multiple sites and projects simultaneously
Valid driver’s license
Ability to travel at least 60% internationally and domestically