Regulatory and Start Up Specialist

IQVIA MedTech Clinical Solutions, specializes in clinical research for Medical Devices and In-Vitro Diagnostic (IVD) products. IQVIA MedTech’s focused expertise meets the growing needs of device Sponsors to justify product safety and effectiveness as well as reimbursement and adoption challenges due to increased scrutiny by regulators, end-users, and...

Study Start Up Specialist, IQVIA Biotech - Italy - Homebased - IQVIA Biotech is looking for an experienced Clinical Study Start-up professional to join our Study Start-Up Unit. - The Study Start-up Specialists are responsible for conducting and facilitating specific start-up activities that may include site identification, feasibility, essential document...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. _Hungarian and English Fluent._ Essential Functions -...

Job Overview Our teams are growing! - We are looking for a Clinical Operation Manager | Regulatory and Start Up Manager to work fully dedicated to one of our biggest sponsor. - This person will direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including...

Webuild is hiring for the Milan Headquarters, a fix-term Procurement Bidding & Startup Specialist to work within its Global Supply Chain Department. Responsibilities include: During the bid-study phase Supporting the Bidding Support & Project Start up team to identify vendors and subcontractors to engage in the market analyses needed to define the bid...

Job OverviewWe are seeking a Clinical Start Up Manager to lead cross-functional project teams globally for assigned studies in the start up phase. The successful candidate will ensure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.Key ResponsibilitiesMonitor study timelines, patient recruitment, and...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Start up Manager office based in Milan. Job Overview Leading cross-functional project...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally.They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access.They are currently seeking a Clinical Start up Manager office based in Milan.Job Overview Leading cross-functional project...

Resourcing Life Science is seeking a Clinical Start Up Manager to lead cross-functional project teams globally for assigned studies in the start up phase. The ideal candidate will ensure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.Key responsibilities include monitoring study timelines, patient...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical Biotech companies globally.They offer a full service solution encompassing clinical non-clinical development, peri-approval market access.They are currently seeking a Clinical Start up Manager office based in Milan.Job Overview Leading cross-functional project teams...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Start up Manager office based in Milan. Job Overview Leading cross-functional...

When our values align, there's no limit to what we can achieve.We are seeking a highly motivated and detail-oriented Regulatory Intelligence Specialist to join our team.As a Regulatory Intelligence Specialist , you will be responsible for Regulatory Intelligence activities, ensuring that Parexel stays up to date with regulatory updates and implements...

390355BR **Study Start-Up Manager - Study & Site Operations**: Italy **About the role** Location: Milan, Italy Full-time, Hybrid, #LI-Hybrid Through trying, learning, and then trying again, we deepen our understanding of how disease affects life, not just health. We create a restored sense of control and possibility for patients and the people around...

Job OverviewResourcing Life Science is seeking a Clinical Start Up Manager to lead cross-functional project teams globally for assigned studies in the start up phase. The ideal candidate will assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.Key ResponsibilitiesMonitor study timelines, patient...

**Regulatory Affairs Specialist (maternity leave)** At AstraZeneca we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As **Regulatory Affairs Specialist (maternity leave)** in...

About EWOR GmbHEWOR GmbH is a premier entrepreneurship platform that empowers outstanding talents and serial entrepreneurs to build and scale their ventures.Salary: €50,000 - €75,000 per annumWe offer a competitive salary package that includes a monthly stipend of up to €6,250 for our start-up founders. This amount may vary based on your individual...

Job SummaryThe Regulatory Affairs Senior Specialist will be supporting the implementation, execution and management of the local regulatory activities in Italy ensuring regulatory compliance with local regulatory requirements and corporate policies.The Regulatory Affairs Senior Specialist supports interactions with the national Regulatory Authorities, i.e....

Webuild, nuovo nome di Salini Impregilo, è un player globale delle costruzioni specializzato nella realizzazione di grandi opere e infrastrutture complesse per la mobilità sostenibile, l’energia idroelettrica, l’acqua, i green buildings, il tunneling. Espressione di 116 anni di esperienza ingegneristica applicata in 50 paesi dei cinque continenti,...

Webuild, nuovo nome di Salini Impregilo, è un player globale delle costruzioni specializzato nella realizzazione di grandi opere e infrastrutture complesse per la mobilità sostenibile, l’energia idroelettrica, l’acqua, i green buildings, il tunneling. Espressione di 116 anni di esperienza ingegneristica applicata in 50 paesi dei cinque continenti,...

**Data**:7 ott 2024 **Location**: Milano, Italia **Società**:Webuild S.p.A. Webuild, nuovo nome di Salini Impregilo, è un player globale delle costruzioni specializzato nella realizzazione di grandi opere e infrastrutture complesse per la mobilità sostenibile, l’energia idroelettrica, l’acqua, i green buildings, il tunneling. Espressione di 117...