As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies
Job Summary
As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
Key responsibilities include assisting in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, 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.
Matching Summary
As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
Clinical trial coordination
Protocol adherence
Regulatory guidelines
Data collection and documentation
Cross-functional collaboration
Nice-to-have
Innovation and excellence
Inclusive environment
Well-being and work-life balance
Commitment to data integrity
Key Requirements
1+ year of relevant experience
Bachelor's degree in scientific or healthcare field