Medical Evidence Advisor Oncology
23 ore fa
Monza, Lombardia, Italia
AstraZeneca
Tempo pieno
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Overview 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) Responsabilità
* 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 Requisiti fondamentali
* 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)
* 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) Responsabilità
* 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 Requisiti fondamentali
* 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)