Overview

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 premio
- 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

📌 Medical Evidence Advisor Oncology (Milano)
🏢 Astrazeneca
📍 Milano