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 Clinical Research Associate II, you will conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance 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
Collaboration with investigators and site staff
Data review and query resolution
Ability to travel at least 60%
Valid driver’s license
Nice-to-have
Oncology experience
Strong organizational and communication skills
Ability to work independently and collaboratively
Inclusive and diverse work environment
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years Clinical Research Associate experience
In-depth knowledge of clinical trial processes and ICH-GCP guidelines