Senior Clinical Research Associate at ICON Plc plays 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
Senior Clinical Research Associate at ICON Plc plays 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 and inclusive culture that rewards high performance and nurtures talent, providing competitive salary and a range of benefits focused on well-being and work-life balance.
The role requires frequent travel and offers opportunities to collaborate with cross-functional teams while supporting site personnel to ensure successful trial execution.
Matching Summary
Senior Clinical Research Associate at ICON Plc plays 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
Travel up to 60% internationally and domestically
Proficiency in clinical trial software
Nice-to-have
Strong organizational and problem-solving skills
Excellent communication and interpersonal skills
Stakeholder management and influence
Training and guidance to site staff
Building effective site relationships
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive CRA experience with clinical trial process knowledge