Clinical Research Associate

As a Clinical Research Associate, you will contribute to routine study monitoring updates. You will perform all aspects of CRA duties including site selection, initiation, monitoring visits, close-out visits, and database lock. In this role, you will be embedded in our client's study team and supported by an ICON line manager. Your responsibilities include overseeing all aspects of study site management to ensure high-quality data, low query levels, and favorable Quality Assurance reports. ICON offers competitive salaries and comprehensive benefits focused on well-being and work-life balance.