As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards
Job Summary
As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality 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 Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.
Skills & Requirements
Must-have
Clinical trial management systems
Site activation and document tracking
Site communication and query resolution
Logistics coordination for site visits
Accurate documentation and filing
Collaborative team environment
Nice-to-have
Process improvement initiatives
Customer-focused site support
Adaptability to changing priorities
Proficiency with MS Office
High attention to detail
Key Requirements
Bachelor’s degree or equivalent experience
Initial experience in clinical research or regulated environment