In this role, you will lead the RWE strategy for prioritized brands in Italy, aligning evidence generation with brand and regional/global agendas to deliver timely insights. You will work at the intersection of medical, market access, and commercial teams to identify evidence gaps and design end-to-end RWE programs across the product lifecycle. Your work translates data into value propositions that support patient access and business goals. A key hook is shaping evidence that accelerates access to transformative medicines within a collaborative oncology setting.annual target premio or incentiveCBA Chemical-Pharmaceuticalsalary range provided (69.475,2 ,80 EUR)Lead RWE strategy for prioritized brands and secure/expand patient accessDesign and prioritise RWE programs across the product lifecyclePartner with Market Access to address pricing, reimbursement and access questionsIntegrate Medical, Market Access and Commercial perspectives to develop value evidenceOversee ESR and AstraZeneca-sponsored observational studies; manage governanceLead end-to-end project management: timelines, budgets, resources, risksDevelop study concepts, protocols, CRFs, and study reports; disseminate via abstracts, posters, manuscriptsCoordinate ESR study drug supply and safety reportingApply methodological expertise across epidemiology, health economics, and outcomes researchEnsure data access, governance, and third-party relationships with data providersEnsure ethics submissions, transparency,



and compliance with policies and standardsNegotiate and manage external partnerships; maintain collaborationsTranslate health outcomes evidence to internal and external stakeholders; communicate findingsCollaborate with global/regional teams to align priorities and deliveryCommunicate complex evidence effectively to scientific and business audiencesScientific degree in a relevant therapeutic area or scientific disciplineSolid understanding of biomedical research and clinical/observational study designHands-on experience in clinical research and evidence-generation studiesKnowledge of clinical research legislation, data protection, and quality/ transparency standardsKnowledge of the Italian healthcare system and evidence needs xysqume of payers/decision-makersProven project leadership and cross-functional delivery experienceStrong written and verbal communication skills; ability to simplify complex evidenceCollaborative, outcome-oriented mindset with stakeholder-management experienceProfessional proficiency in English (spoken and written)Proficiency in Microsoft Office (Excel and PowerPoint)outcome-orientedstakeholder-managementmethodological expertise in epidemiology, statistics, health economics and outcomes researchdata access and stewardship; governance and data protectionexperience with real-world data sources (electronic health records, claims, registries)Medical Evidence Advisor Oncology pavia, lombardia, it#J-18808-Ljbffr

📌 Medical Evidence Advisor Oncology (Bardi)
🏢 AstraZeneca
📍 Bardi