Medical Evidence Advisor Oncology
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.
annual target premio or incentive
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)
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)
Medical Evidence Advisor Oncology pavia, lombardia, it
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 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)
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)
Medical Evidence Advisor Oncology pavia, lombardia, it