The Clinical and Ancillary Supplies Services (CASS) Specialist I supports the delivery of the clinical and ancillary supplies component of assigned studies within a country or region.
Act as contact with the study team during clinical and ancillary start-up activities, provide input to the development of the Clinical Trial Supplies Plan or Clinical Trial Supply Flow for a given group of countries, perform and coordinate label review and country translations, and ensure required documentation and processes related to supply management are communicated and obtained.
Serve as the key contact for importation logistics and document exchange, provide consultancy on supply distribution strategy, and maintain project-specific clinical and ancillary supply logistics. Work closely with drug and ancillary supply distribution, IVRS/IRT, and label translation vendors during set-up and maintenance of related logistics.