Clinical Data

Overview As a Clinical Safety Specialist at Medtronic, you’ll collaborate to design, document, and implement clinical data collection studies and safety-focused data review. You will develop protocols and data systems, organize data for analysis, and resolve data discrepancies to support regulatory-compliant reporting. Your input will shape protocol...

Medtronic in Italy seeks a Clinical Safety Specialist to design, document, and implement clinical data collection studies and safety-focused data review.Prima di candidarsi per questo ruolo, la preghiamo di leggere le seguenti informazioni su questa opportunità, riportate di seguito.You will develop protocols and data systems, organize data for analysis,...

Medtronic in Italy seeks a Clinical Safety Specialist to design, document, and implement clinical data collection studies and safety-focused data review. You will develop protocols and data systems, organize data for analysis, and resolve discrepancies to support regulatory reporting.Collaborate with stakeholders across projects to drive safety outcomes,...

As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your work...

As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your work...

OverviewIn this role you will advance clinical studies by leading on-site and remote monitoring, ensuring data integrity and site partnership. You will drive study ownership across multiple sponsors and therapeutic areas, with a focus on deeper study knowledge and strong site relationships in Italy. You’ll mentor less experienced CRAs and operate in a...

OverviewIn this role you guide trial sites through the cell therapy journey, translating complex protocols into practical actions that improve feasibility, start-up speed, and study conduct. You partner with cross-functional teams to align strategies, share scientific insights, and drive execution quality across regions. You shape site readiness, training,...

OverviewIn this role you will provide strategic legal support for European R&D activities and select markets, partnering with regional and global teams to navigate clinical trials, regulatory, data privacy, and vendor relations. You will translate complex regulations into practical risk mitigations while supporting global programs across diverse...

OverviewJoin Allucent as a Start-Up Associate II to lead local site start-up activities for clinical trials. You will coordinate regulatory and ethics submissions and serve as the primary point of contact with authorities, investigators, and sites through the initial study phase. You will manage documentation, timelines, and country-specific requirements to...