ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
As a Clinical Research Associate I/II, you will conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and data integrity.
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 committed to innovation and excellence.
Skills & Requirements
Must-have
Clinical trial monitoring and site visits
Protocol compliance and patient safety
Data review and query resolution
Collaboration with investigators and site staff
Fluent English and Turkish
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 2 years experience as Clinical Research Associate
In-depth knowledge of clinical trial processes and ICH-GCP guidelines