26 ott - Monza
AstraZeneca
OverviewIn 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.Retribuzione / Benefitsannual target premiowellbeing benefitsfull-time permanent positionResponsabilitàDefine and lead the RWE strategy for prioritized brands to secure and expand patient accessDesign and prioritize RWE programs across the product lifecycle aligned with brand, regional and global prioritiesPartner with Market Access to address pricing, reimbursement and access questions with robust research methodsCoordinate cross-functional input from Medical, Market Access and Commercial to develop value evidenceOversee ESR and AstraZeneca-sponsored observational studies, including governance and feasibility assessmentsLead end-to-end project management: timelines, budgets, resources, risks, dependenciesDevelop study concepts, protocols, CRFs and reports; disseminate via abstracts, posters and publicationsCoordinate ESR operations and safety, including study drug supply and safety reportingApply diverse methodological approaches (epidemiology, health economics, outcomes research)Identify data sources,
manage third-party data providers and ensure data governanceEnsure research quality, ethics, transparency and compliance with PoliciesLead ethics submissions and ensure results disclosure in line with policiesNegotiate and manage external collaborations and data-provider contractsCollaborate globally/regionally to align evidence priorities and share best practicesTranslate health-outcomes evidence to internal and external audiences and present findings in scientific settingsRequisiti fondamentaliScientific degree in a relevant therapeutic area or scientific disciplineSolid understanding of biomedical research, drug development and clinical environmentHands-on experience in clinical research and in evidence-generation study design or interpretationKnowledge of clinical xysqume research legislation, ethics, data protection and quality/ transparency standardsKnowledge of the Italian healthcare system and evidence needs of payers and decision-makersDemonstrated project leadership and cross-functional deliveryStrong written and verbal communication skills; ability to present to scientific and business audiencesCollaborative, outcome-oriented mindset with stakeholder-management skillsProfessional proficiency in English (spoken and written)Proficiency in Microsoft Office, especially Excel and PowerPointCollaborativeStakeholder managementResults-orientedStatistical and epidemiological methods for observational researchHealth economics and outcomes researchData access, governance and protection#J-18808-Ljbffr
27 ott - Rodengo-saiano
ADHR Group
27 ott - Cesena
Archimede
27 ott - Campo di Ne
E-Work S. P. A.
27 ott - Varese
Manpower Saronno Tommaseo