Medical Evidence Advisor Oncology
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. annual target premio or incentive CBA Chemical-Pharmaceutical 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 Lead end-to-end project management: timelines, budgets, resources, risks 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 maintain collaborations Translate health outcomes evidence to internal and external stakeholders; Collaborate with global/regional teams to align priorities and delivery 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 Collaborative, outcome-oriented mindset with stakeholder-management experience Professional proficiency in English (spoken and written) Proficiency in Microsoft Office (Excel and PowerPoint) 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) Medical Evidence Advisor Oncology pavia, lombardia, it #
and third-party relationships with data providers maintain collaborations Translate health outcomes evidence to internal and external stakeholders; Collaborate with global/regional teams to align priorities and delivery 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 Collaborative, outcome-oriented mindset with stakeholder-management experience Professional proficiency in English (spoken and written) Proficiency in Microsoft Office (Excel and PowerPoint) 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) Medical Evidence Advisor Oncology pavia, lombardia, it #