Medical Evidence Advisor Oncology
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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 bonus
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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