Experteer Overview Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. In this role you support the global study team across the full study lifecycle, from CSP development to study set-up, maintenance, close-out, CSR development, and archiving. You collaborate with internal and external partners to execute delegated study aspects, maintain timelines and quality, and oversee vendor-related activities. You contribute to planning and governance, mentor colleagues, and help manage budgets and risks. This position blends cross-functional coordination with proactive problem-solving in a dynamic clinical research environment.Compensaciones / Incentivos• Support clinical study execution with cross-functional teams to meet timelines and quality standards• Prepare study documents and vendor-related materials, including the Vendor Oversight Plan• Maintain effective interactions with Data Management, Procurement, Regulatory, Patient Safety,



and QA• Collaborate with internal and external partners to deliver delegated study aspects• Plan and participate in internal and external meetings• Identify risks/issues and contribute to mitigation plans• Support GSM with project and budget management within delegation• Engage in departmental initiatives and SME functions• Mentor team members and foster a collaborative work environment• Provide support for other study and functional activities as xqbhyrx assignedResponsabilidades• Bachelor's degree or equivalent in clinical practice/health care, life sciences, or drug development, or equivalent experience• Proficiency with Microsoft Office (Excel, PowerPoint, SharePoint Online), eTMF, and Veeva Systems• Excellent organizational, communication, and time management skills• Highly proactive with initiative-taking• Strong relationship-building skillsRequisitos principales•

📌 Global Study Associate Manager (Barcelona)
🏢 Alexion Pharmaceuticals
📍 Barcelona