Regulatory Start-Up Associate II

Allucent seeks a Start-Up Associate II in Italy to coordinate local site start-up activities and manage regulatory submissions with RA/IEC/IRB, acting as the main point of contact for investigators and sites through early study phases.You will file documents in eTMF, prepare country-specific CTAs and budgets, negotiate with sites, and support the Global...

Allucent seeks a Start-Up Associate II in Italy to coordinate local site start-up activities and manage regulatory submissions with RA/IEC/IRB, acting as the main point of contact for investigators and sites through early study phases.You will file documents in eTMF, prepare country-specific CTAs and budgets, negotiate with sites, and support the Global...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site...

Allucent seeks a Start-Up Associate II in Italy to coordinate local site start-up activities and manage regulatory submissions with RA/IEC/IRB, acting as the main point of contact for investigators and sites through early study phases.You will file documents in eTMF, prepare country-specific CTAs and budgets, negotiate with sites, and support the Global...

OverviewAs an RSU Specialist, you will lead country-specific site activation and regulatory activities within IQVIA's FSP team in Italy. You will act as the primary liaison for investigative sites and project teams, ensuring compliant, timely site activation and regulatory documentation. You will leverage local regulatory expertise to support timelines, risk...

Centrocliniconemo a Milano ricerca un/a Start-Up & Regulatory Affairs Officer per la ricerca in ambito clinico. Il candidato ideale possiede una laurea in discipline scientifiche e ha esperienza nella ricerca clinica. Sarà responsabile della valutazione della fattibilità degli studi, della gestione dei contratti e del mantenimento della documentazione...

Start-Up & Regulatory Affairs Officer – Observational StudiePosizione: Start-Up & Regulatory Affairs Officer - Observational StudieContratto: partita IVASede di lavoro: Centro Clinico Nemo Milano, Ospedale NiguardaCompenso: 25.000 euroRequisitilaurea in discipline scientifiche, quali biologia, biotecnologie, farmacia, scienze infermieristiche,...