Medical Evidence Advisor Oncology

25 ott - Monza
AstraZeneca

h3Overview /h3pIn this role you lead the real-world evidence (RWE) strategy for prioritized oncology brands in Italy, aligning evidence generation with brand objectives and regional/global priorities. You’ll collaborate across 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 scientific advancement. You will drive high-impact studies, governance, and dissemination to inform decisions and shape cancer care. /ph3Retribuzione / Benefits /h3ulliannual target premio /liliwellbeing benefits /lilifull-time permanent position /li /ulh3Responsabilità /h3ulliDefine and lead the RWE strategy for prioritized brands to secure and expand patient access /liliDesign and prioritize RWE programs across the product lifecycle aligned with brand, regional and global priorities /liliPartner with Market Access to address pricing, reimbursement and access questions with robust research methods /liliCoordinate cross-functional input from Medical, Market Access and Commercial to develop value evidence /liliOversee ESR and AstraZeneca-sponsored observational studies, including governance and feasibility assessments /liliLead end-to-end project management: timelines, budgets, resources, risks, dependencies /liliDevelop study concepts, protocols, CRFs and reports; disseminate via abstracts, posters and publications /liliCoordinate ESR operations and safety, including study drug supply and safety reporting /liliApply diverse methodological approaches (epidemiology, health economics, outcomes research) /liliIdentify data sources,



manage third-party data providers and ensure data governance /liliEnsure research quality, ethics, transparency and compliance with Policies /liliLead ethics submissions and ensure results disclosure in line with policies /liliNegotiate and manage external collaborations and data-provider contracts /liliCollaborate globally/regionally to align evidence priorities and share best practices /liliTranslate health-outcomes evidence to internal and external audiences and present findings in scientific settings /li /ulh3Requisiti fondamentali /h3ulliScientific degree in a relevant therapeutic area or scientific discipline /liliSolid understanding of biomedical research, drug development and clinical environment /liliHands-on experience in clinical research and in evidence-generation study design or interpretation /liliKnowledge of clinical research legislation, ethics, data protection and quality/ transparency standards /liliKnowledge of the Italian healthcare system and evidence needs of payers and decision-makers /liliDemonstrated project leadership and cross-functional delivery /liliStrong written and verbal communication skills; ability to present to scientific and business audiences /liliCollaborative, outcome-oriented mindset with stakeholder-management skills /liliProfessional proficiency in English (spoken and written) /liliProficiency in Microsoft Office, especially Excel and PowerPoint /liliCollaborative /liliStakeholder management /liliResults-oriented /liliStatistical and epidemiological methods for observational research /liliHealth economics and outcomes research /liliData access, governance and protection /li /ul #J-18808-Ljbffr

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