Director, US HEOR & RWE

Location

United States

Posted

84 days ago

Salary

0

No structured requirement data.

Job Description

Director, US HEOR & RWE

Zealand Pharma

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description The US Director, HEOR & RWE will lead the design, execution, and communication of health, economic and outcomes research strategies supporting the company’s global metabolic health portfolio. This leader will generate high-quality real-world, clinical, and economic evidence to demonstrate product value to payers, providers, patients, and policymakers. The role requires expertise in value demonstration, real-world data (RWD), and outcomes modeling, as well as the ability to translate complex data into actionable insights for commercial and clinical decision-making. Remote location, ideally NE corridor. - Develop and implement integrated global HEOR strategies to support pipeline and lifecycle management programs with a US launch focus. - Lead development of US RWD strategies and partnerships with academic consortia, claims databases, and health systems to support value demonstration, comparative effectiveness, and longitudinal outcomes studies. - Design and implement real-world data analyses to understand and articulate the current patient demographics, treatment patterns, and outcomes. - Develop AMCP value dossiers, economic modeling, narratives, and scientific publications to support value propositions. - Serve as a key domain expert for payer engagement, providing evidence summaries and presentations that strengthen product positioning and formulary access. - Engage and collaborate with external partners including payers, providers, and other access decision-makers to establish/maintain strong partnerships and gather insights. - Lead the external dissemination of HEOR/RWE deliverables including publications, presentations, and professional conferences. - Provide input to clinical development programs. - Collaborate closely with partners on HEOR & RWE programs, ensuring coordinated evidence generation, cost-sharing, and data-sharing aligned to global commercialization goals. - Represent HEOR in relevant governance meetings, advisory boards, and internal strategy sessions to shape business decisions through evidence-driven insight. Qualifications - PhD, PharmD, MPH, or Master’s in Health Economics, Outcomes Research, Epidemiology, or a related discipline. - 8–12 years of HEOR/RWE experience in biotech, pharmaceutical organizations or consultancies with demonstrated success in pre-launch and commercialization phases. - Therapeutic area expertise in metabolic, endocrine, or cardiometabolic diseases strongly preferred. - Deep understanding of payer and evidence requirements in the U.S. - Proficiency in RWD study design and analysis, and patient outcome measure development. - Proven ability to communicate complex data to non-technical audiences, including payers, regulators, and cross-functional business leaders. - Experience leading external collaborators, vendors, and cross-company joint HEOR initiatives. - Publication track record and presentation experience at peer-reviewed scientific meetings. Company Description Zealand Pharma A/S (Nasdaq: ZEAL) is a biotechnology company focused on the discovery and development of peptide-based medicines. More than 10 drug candidates invented by Zealand Pharma have advanced into clinical development, of which two have reached the market and three candidates are in late-stage development. The company has development partnerships with a number of pharma companies as well as commercial partnerships for its marketed products. Zealand Pharma was founded in 1998 and is headquartered in Copenhagen, Denmark, with a team in the U.S.

Job Requirements

  • PhD, PharmD, MPH, or Master’s in Health Economics, Outcomes Research, Epidemiology, or a related discipline.
  • 8–12 years of HEOR/RWE experience in biotech, pharmaceutical organizations or consultancies with demonstrated success in pre-launch and commercialization phases.
  • Therapeutic area expertise in metabolic, endocrine, or cardiometabolic diseases strongly preferred.
  • Deep understanding of payer and evidence requirements in the U.S.
  • Proficiency in RWD study design and analysis, and patient outcome measure development.
  • Proven ability to communicate complex data to non-technical audiences, including payers, regulators, and cross-functional business leaders.
  • Experience leading external collaborators, vendors, and cross-company joint HEOR initiatives.
  • Publication track record and presentation experience at peer-reviewed scientific meetings.

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