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.
The role involves conducting 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 committed to innovation and excellence.
Skills & Requirements
Must-have
Clinical trial site monitoring
Protocol compliance assurance
Data review and query resolution
Travel at least 60% internationally and domestically
Valid driver’s license required
Nice-to-have
Strong organizational skills
Effective communication skills
Ability to work independently and collaboratively
Attention to detail
Inclusive and diverse work culture
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 guidelines