Senior Clinical Team Manager — Start-Up

Novo Nordisk in Rome is seeking a Clinical Trial Administrator to keep clinical trials in Italy moving with accuracy and pace.Si assicuri di leggere l'intera descrizione riportata di seguito e di candidarsi immediatamente se è sicuro/a di soddisfare tutti i requisiti.You will support the local study team from start-up to close-out, managing trial...

Novo Nordisk in Rome is seeking a Clinical Trial Administrator to keep clinical trials in Italy moving with accuracy and pace. You will support the local study team from start-up to close-out, managing trial documentation, tracking progress, coordinating vendors, and ensuring investigator site payments are on time. The role requires a Master’s degree in...

Novo Nordisk in Rome is seeking a Clinical Trial Administrator to keep clinical trials in Italy moving with accuracy and pace. You will support the local study team from start-up to close-out, managing trial documentation, tracking progress, coordinating vendors, and ensuring investigator site payments are on time.The role requires a Master’s degree in...

Novo Nordisk in Rome is seeking a Clinical Trial Administrator to keep clinical trials in Italy moving with accuracy and pace. You will support the local study team from start-up to close-out, managing trial documentation, tracking progress, coordinating vendors, and ensuring investigator site payments are on time.The role requires a Master’s degree in...

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

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...

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.Qualifiche, competenze e l'esperienza necessaria per questo ruolo sono disponibili nella descrizione completa riportata di seguito.In this role...

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...