Medical Evidence Advisor Oncology
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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.
Retribuzione / Benefits- annual target bonus or incentive
- wellbeing benefits
- full-time; permanent position
- location: Milan, Italy
- CBA Chemical-Pharmaceutical
- salary range provided (69.475,20 - 104.212,80 EUR)
- Lead RWE strategy for prioritized brands and secure/expand patient access
- Design and prioritise RWE programs across the product lifecycle
- Partner with Market Access to address pricing, reimbursement and access questions
- Integrate Medical, Market Access and Commercial perspectives to develop value evidence
- Oversee ESR and AstraZeneca-sponsored observational studies; manage governance
- Lead end-to-end project management: timelines, budgets, resources, risks
- Develop study concepts, protocols, CRFs, and study reports; disseminate via abstracts, posters, manuscripts
- Coordinate ESR study drug supply and safety reporting
- Apply methodological expertise across epidemiology, health economics, and outcomes research
- Ensure data access, governance, and third-party relationships with data providers
- Ensure ethics submissions, transparency, and compliance with policies and standards
- Negotiate and manage external partnerships; maintain collaborations
- Translate health outcomes evidence to internal and external stakeholders; communicate findings
- Collaborate with global/regional teams to align priorities and delivery
- Communicate complex evidence effectively to scientific and business audiences
- Scientific degree in a relevant therapeutic area or scientific discipline
- Solid understanding of biomedical research and clinical/observational study design
- Hands-on experience in clinical research and evidence-generation studies
- Knowledge of clinical research legislation, data protection, and quality/ transparency standards
- Knowledge of the Italian healthcare system and evidence needs of payers/decision-makers
- Proven project leadership and cross-functional delivery experience
- Strong written and verbal communication skills; ability to simplify complex evidence
- Collaborative, outcome-oriented mindset with stakeholder-management experience
- Professional proficiency in English (spoken and written)
- Proficiency in Microsoft Office (Excel and PowerPoint)
- collaborative
- outcome-oriented
- stakeholder-management
- methodological expertise in epidemiology, statistics, health economics and outcomes research
- data access and stewardship; governance and data protection
- experience with real-world data sources (electronic health records, claims, registries)
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