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Global Director of Rare Disease Treatment Access

2 months ago


Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS - Nn1 Full time
About the Role

We are seeking a highly skilled and experienced professional to lead our Health Economics and Outcomes Research (HEOR) efforts for rare diseases. As the Global Director of Rare Disease Treatment Access, you will play a critical role in shaping our strategies and plans to ensure that our treatments are accessible and valued by patients and healthcare systems worldwide.

Key Responsibilities
  1. Develop and Implement HEOR Strategies: Lead the development of health economic models, economic evaluations, budget impact studies, quality-of-life studies, and indirect treatment comparisons to inform our business decisions.
  2. Collaborate with Cross-Functional Teams: Work closely with Research and Development, Medical, Biostatistics, Commercial, and other stakeholders to ensure alignment and effective communication.
  3. Market Access and Pricing Alignment: Collaborate with the Market Access and Pricing team to develop strategies and materials that support regional and country-level access to our treatments.
  4. Global Reimbursement Dossier Development: Develop and maintain the Global Reimbursement Dossier, ensuring that affiliates have access to HEOR data and resources.
Requirements
  1. Master's Degree in Health Economics or Outcomes Research: A master's degree in a relevant field is required.
  2. Experience in Health Economics and Outcomes Research: A minimum of 5 years of experience in HEOR within the pharmaceutical or healthcare industry is required.
  3. Indirect Therapeutic Comparison (ITC) Expertise: A good understanding of ITC methods and analysis is essential.
  4. Complex Matrix Management: Proven experience in building and managing complex matrices in a professional setting is required.
  5. Fluency in English: Fluency in written and verbal English is necessary.
About the Department

The Rare Blood Disorders Market Access and Pricing team is a dedicated group of professionals working to ensure global access to our treatments for patients with Haemophilia, Sickle Cell Disease, and Thalassemia. We collaborate closely with senior leadership and other cross-functional teams to drive innovation and achieve our goals.