23 ott - Monza
Astrazeneca
Overview In 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 / Benefits
annual target premio wellbeing benefits full-time permanent position
Responsabilità
Define and lead the RWE strategy for prioritized brands to secure and expand patient access Design and prioritize RWE programs across the product lifecycle aligned with brand, regional and global priorities Partner with Market Access to address pricing, reimbursement and access questions with robust research methods Coordinate cross-functional input from Medical, Market Access and Commercial to develop value evidence Oversee ESR and AstraZeneca-sponsored observational studies, including governance and feasibility assessments Lead end-to-end project management: timelines, budgets, resources, risks, dependencies Develop study concepts, protocols, CRFs and reports; disseminate via abstracts, posters and publications Coordinate ESR operations and safety, including study drug supply and safety reporting Apply diverse methodological approaches (epidemiology, health economics, outcomes research) Identify data sources,
manage third-party data providers and ensure data governance Ensure research quality, ethics, transparency and compliance with Policies Lead ethics submissions and ensure results disclosure in line with policies Negotiate and manage external collaborations and data-provider contracts Collaborate globally/regionally to align evidence priorities and share best practices Translate health-outcomes evidence to internal and external audiences and present findings in scientific settings
Requisiti fondamentali
Scientific degree in a relevant therapeutic area or scientific discipline Solid understanding of biomedical research, drug development and clinical environment Hands-on experience in clinical research and in evidence-generation study design or interpretation Knowledge of clinical research legislation, ethics, data protection and quality/ transparency standards Knowledge of the Italian healthcare system and evidence needs of payers and decision-makers Demonstrated project leadership and cross-functional delivery Strong written and verbal communication skills; ability to present to scientific and business audiences Collaborative, outcome-oriented mindset with stakeholder-management skills Professional proficiency in English (spoken and written) Proficiency in Microsoft Office, especially Excel and PowerPoint Collaborative Stakeholder management Results-oriented Statistical and epidemiological methods for observational research Health economics and outcomes research Data access, governance and protection
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