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.
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
clinical trial monitoring and site visits
protocol compliance and data integrity
ICH-GCP guidelines knowledge
travel at least 60% internationally and domestically
valid driver’s license required
Nice-to-have
strong organizational and communication skills
ability to work independently and collaboratively
attention to detail
inclusive and diverse work environment
Key Requirements
Bachelor's degree in scientific or healthcare-related field
minimum 4 years Clinical Research Associate experience
in-depth knowledge of clinical trial processes and regulations