Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essen...
clinical studies. As a PPD CRA, you will perform and coordinate all aspects of the clinical monitoring and site management.... Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls...
at least 2 years of year of on-site monitoring experience. - Equivalent combination of education, training and experience may...
with a CRO, including at least 2 years of experience leading regulatory/start-up project teams; - Knowledge and experience... amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization...
in clinical studies - Minimum of 2 years as a successful Clinical Trial Manager; or > 4 years for a Senior Clinical Trial.... - Review and approve trip reports and follow-up letters within required timeframe. - Schedule and manage weekly CRA project...