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Allucent
Allucent is seeking a Start-Up Associate II to join our A-team in Italy, with hybrid/remote options. The SUA coordinates local site start-up activities, handles regulatory submissions to RA/IEC/IRB, and serves as main communicator to investigators and sites through the initial phase of a clinical study. This role supports document management, regulatory and ethical submissions, and interaction with authorities, while ensuring compliance and timely updates across CTMS and study teams. #J-18808-Ljbffr
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