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Ipsen

Global Health Economics & Outcomes Research (HEOR) Director

Paris
Posted 1 day ago
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Global Health Economics & Outcomes Research (HEOR) Director

Company:

Ipsen Biopharm Ltd

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease, and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France, and the U.K., we tackle areas of high unmet medical need through research and innovation.

Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence, and impact. At Ipsen, every individual is empowered to be their true selves, grow, and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

Job Description:

SUMMARY OF THE POSITION

The Director Global HEOR will be part of the Global Value & Access Team collaborating closely with colleagues in Market Access & Pricing, Marketing, Clinical Development, Research and Development, Market Research, Regulatory Affairs, Medical Affairs, and Strategic Planning, to deliver critical strategic value evidence generation in support of access to Ipsen’s products spanning early development, launch, and mature phases across Oncology, Neuroscience, and Rare disease therapeutic areas. The initial assignment will be in the Rare disease area, but future opportunities may involve assignment across other therapeutic areas of Ipsen portfolio.

This is an exciting opportunity for an experienced HEOR professional to leverage strategic and technical understanding of HEOR in an international setting leading value evidence generation on Ipsen product portfolio for payers and other key stakeholders worldwide.

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MAIN RESPONSIBILITIES

  • Lead launch readiness and post-launch updates and development of core HEOR/Access deliverables including systematic and targeted literature reviews, burden of illness studies, unmet medical needs, clinical and patient-relevant outcomes, clinical guidelines, comparative effectiveness including evidence synthesis (including indirect treatment comparisons and network meta-analyses), Cost-Effectiveness Analysis models, Budget Impact Analysis models, Global Value Dossiers, Payer/Product Value Propositions, Objection Handlers for Ipsen products.
  • Lead EU HTA Regulation JCA planning and execution as applicable aligned with product assignments.
  • Support Payer value evidence communication through presentation of abstracts/posters of key work at clinical and HEOR conferences and manuscript publications.
  • Contribute to development, updates, and execution of cross-functional Integrated Evidence Generation Plans for Ipsen products working with cross-functional teams ensuring strategic alignment of planned and ongoing HEOR activities.
  • Lead and inform RWE, health outcomes/Patient-reported outcomes strategy and execution supporting development of a compelling Value proposition for payers and other key stakeholders.
  • Lead and inform pipeline target product and value profile and clinical development plans including payer-relevant endpoint in clinical trials.
  • Support development of pricing policy and market access of the company products.
  • Work collaboratively with local affiliates and global cross-functional team including but not limited to Global Medical Affairs, Global Regulatory Affairs, Clinical, Biostatistics, Public Affairs, Marketing, etc.
  • Stay abreast of the evolving payer/HTA landscape in terms of policies, guidelines, and trends leveraging up-to-date knowledge in strategic HEOR planning.
  • Provide training to local country colleagues on value evidence for local adaptation and use.

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SKILLS & EDUCATION

  • A postgraduate degree in health economics or related quantitative discipline.
  • At least 8 years’ relevant experience in the field of HEOR in pharma industry, consultancy, or Academia, in an international setting.
  • Experience working on international HTA submissions.
  • Strong scientific analysis, interpretative, and writing skills.
  • Knowledge of international health care systems.
  • Expertise on HEOR from Oncology, Rare Disease, and/or Neuroscience including evidence synthesis, cost-effectiveness, and budget impact modeling, RWE methodologies for outcomes research and PROs.
  • Knowledge of trial design and understanding of key clinical, PRO, and resource utilization endpoints.

#LI-Hybrid

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.

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Skills

Health Economics
Outcomes Research
Evidence Synthesis
Cost-Effectiveness Analysis
Budget Impact Analysis
Real World Evidence
Patient-Reported Outcomes
HTA Submissions
Value Propositions
Literature Reviews
Clinical Trial Design
Strategic Planning
Market Access
Scientific Writing
Quantitative Analysis
Stakeholder Management

Location

Paris, Ile-de-France, France

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