Start-Up Regulatory Specialist II

Overview As 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,...

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. In this role your key tasks will include: * Track relevant information, data, progress and milestones in CTMS and/or other tracking tools covering...

Medicine moves forward here. So willyou.Per essere preso/a in considerazione per un colloquio, la preghiamo di assicurarsi che la sua candidatura sia pienamente in linea con le specifiche del lavoro riportate di seguito.Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most...

Medicine moves forward here. So willyou.Per essere preso/a in considerazione per un colloquio, la preghiamo di assicurarsi che la sua candidatura sia pienamente in linea con le specifiche del lavoro riportate di seguito.Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most...

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 is seeking an experienced Regulatory Affairs Coordinator to support site start-up activities for clinical trials. You will manage regulatory documents, track milestones in CTMS/eTMF, and prepare local submissions to regulators in coordination with the Global Regulatory team. A Life Science degree and 2+ years in regulatory affairs are required,...

Webuild è alla ricerca di un/aProcurement Specialist | Bidding & Project Start-upper la propria sede diMilano, da inserire nel repartoGlobal Supply Chain. Responsabilità principali Fase di studio dell'offerta: * Identificare, sotto la supervisione del Responsabile del supporto alle gare d'appalto e all'avvio dei progetti, i fornitori e gli appaltatori da...

Allucent is seeking an experienced Regulatory Affairs Coordinator to support site start-up activities for clinical trials. You will manage regulatory documents, track milestones in CTMS/eTMF, and prepare local submissions to regulators in coordination with the Global Regulatory team. A Life Science degree and 2+ years in regulatory affairs are required, with...

At AllucentTM, 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. In this role your key tasks will include: Track relevant information, data, progress and milestones in CTMS and/or other tracking tools covering...