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 for clinical trials while ensuring patient safety and data quality.
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
Phase 1 clinical trial monitoring
Protocol compliance and data integrity
Site qualification and initiation visits
Travel availability at least 60%
Valid driver’s license required
Nice-to-have
Strong organizational and communication skills
Ability to work independently and collaboratively
Attention to detail
Experience with ICH-GCP guidelines
Key Requirements
Bachelor's degree in scientific or healthcare field
Minimum 2 years CRA experience with Phase 1 studies
Residency in NY, NJ, PA, NH, CT, RI, ME, VT, or MA