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 role involves conducting site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance, data integrity, and patient safety throughout clinical trials.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.
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
clinical trial site monitoring
protocol compliance assurance
data integrity management
patient safety oversight
international and domestic travel
valid driver’s license
Nice-to-have
strong organizational skills
effective communication skills
ability to work independently
collaborative team player
attention to detail
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years Clinical Research Associate experience
In-depth knowledge of clinical trial regulations and ICH-GCP