Start-Up Regulatory Specialist II
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.
This role supports document management, regulatory and ethical submissions, and interaction with authorities, while ensuring compliance and timely updates across CTMS and study teams.