The Clinical Research Associate I (CRA I) role is integral to ensuring project success as part of a multi-disciplinary team that provides scientific, statistical, and operations and management support for clinical trials.
This position will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Rho Standard Operating Procedures. The CRA I will be responsible for supporting study team management, providing input into monitoring tool and process development, as well as training for newly assigned project CRAs.
This position requires up to 80% travel and is based in Durham, NC. This is an office-based position.