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.
The Clinical Site Associate plays a pivotal role in supporting clinical trial operations by ensuring site compliance, maintaining accurate documentation, and supporting audit and inspection readiness.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global 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-level communications management
clinical trial documentation maintenance
support audit and inspection readiness
coordinate site trainings and systems access
collaborate with Clinical Research Associates
Nice-to-have
strong organizational and communication skills
ability to work independently and collaboratively
attention to detail and task prioritization
inclusive and accessible work environment
Key Requirements
minimum one year experience as Study Coordinator
Bachelor’s degree in Life Sciences or Healthcare
experience in clinical research or related field preferred