ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
As a Site Management Associate I, you will assist in monitoring clinical trial sites, ensuring adherence to protocols and regulatory requirements while providing essential administrative support.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Site monitoring activities
Compliance with study protocols
Good Clinical Practice (GCP) guidelines
Documentation preparation and data entry
Tracking site performance metrics
Nice-to-have
Strong organizational skills
Excellent communication skills
Collaborative team environment
Basic clinical trial process knowledge
Key Requirements
Bachelor’s degree in relevant field
Some clinical research or site management experience preferred