Medical Evidence Advisor Oncology

1 giorno fa

monzabrianza, lombardia, Italia AstraZeneca Tempo pieno
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 bonus
  • 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