Director Health Economics

Vor 2 Tagen

Basel, Schweiz CTC Resourcing Solutions Vollzeit

For our client, a pharmaceutical company located in Basel, Switzerland, we are looking for a

**Director, Health Economics & Outcome Research (HEOR)**

Your responsibilities would inlcude but are not limited to:

- Responsible for developing HE models during the clinical development of new products, starting at early stages (Ph II/III clinical studies), across multiple therapeutic areas.
- Provide medico-economic and humanistic inputs into the value evidence dossier for each product in clinical development, in collaboration with the respective teams - Market Access, Medical Affairs (e.g., Ph IV studies), Management and further units if needed.
- Design HEOR models and analyses in view of HTA and reimbursement goals for the company's products in Europe, US and the rest of the world.
- At different stages of a drug's development, coordinate systematic literature reviews.
- Provide advice on highest value outcome measures - incl patient reported outcomes -during Ph II/III/IV studies.
- Bridge clinical development approaches with market access & pricing activities.
- Collaborate with the commercial department in setting up real-world evidence studies.
- Actively participate in publication efforts and external scientific presentations
- Support the company in their discussions with authorities and organisms assessing the added value of new medicinal products
- Be part of the Strategic Development team
- Keep up with international developments in the field of pharmacoeconomic and OR

Your qualifications
- Master (and/or PhD) in HE or a related degree and with HTA and OR experience
- Minimum of 5 years job relevant experience with pharmaceutical industry, either as an active and frequent consultant or an employee; direct knowledge of comparative European and US approaches for value evidence generation
- Mastery and practical use experience of health economic models, including relevant statistical skills
- Proven record of successful submission of HTA or value dossiers to relevant bodies, for medicinal products and devices
- Capacity to capture the scientific/medical components of a new drug development program; experience several therapeutic areas
- Direct experience with patient reported outcomes
- Excellent oral and written communication skills and command of English
- Demonstrated ability to work hands-on and autonomously in a fast-paced environment, prioritize multiple competing tasks
- Ability to inspire and convince others

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