Director, HTA, Value & Evidence, Lung Cancer

Scorpion Therapeutics

Cambridge (MA)

On-site

USD 150,000 - 190,000

Full time

14 days+
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Job summary

Scorpion Therapeutics is seeking a senior HEOR leader to drive the US evidence generation strategy for lung cancer and precision medicine in Oncology. You will coordinate inputs across Medical, Market Access, and cross-functional partners to shape launch and lifecycle evidence plans.

The role requires deep HEOR expertise, extensive experience in health economic modeling and real-world evidence, and collaboration with global teams to develop AMCP dossiers and reimbursement-ready tools.

Qualifications

  • Graduate degree required (MSc/MPH/PhD).
  • 7+ years with MSc/MPH/MBA; or 5+ years with PharmD/PhD in HEOR or related fields.
  • Deep understanding of health services research methods (health economic modeling, PROs, statistics, real-world evidence/registries/observational design).
  • Knowledge of drug development and US healthcare/economic environment.

Responsibilities

  • Lead development of the US evidence generation strategy for the lung cancer & precision medicine portfolio in Oncology.
  • Coordinate inputs from US Medical, field-facing colleagues, US Market Access, cross-alliance partners, GASP and USMA to define evidence needs and integrate the strategy for launch and lifecycle.
  • Design and execute HEOR studies including site engagement, chart abstraction, and retrospective data collection from concept through publication.
  • Develop US value & evidence strategy with US Medical and Global HV&E, including AMCP dossiers, systematic literature reviews, economic models, and tools for reimbursement and access.
  • Provide strategic input into clinical trial designs and PRO data analysis/interpretation to support reimbursement and access negotiations.
  • Ensure dissemination of HEOR materials per regulatory guidance/internal SOPs (e.g., PVPs, promotional materials, FDAMA 114-compliant materials).
  • Build external research collaborations with experts, healthcare policy makers, payers, and academic/community oncology settings.

Skills

HEOR expertise
Health economic modeling
PRO data analysis
Real-world evidence
Independent project management

Education

MSc/MPH/PhD
MBA

Job description

Role Responsibilities:
  • Lead development of the US evidence generation strategy for the lung cancer & precision medicine portfolio in Oncology.
  • Coordinate inputs from US Medical, field-facing colleagues, US Market Access, cross-alliance partners, GASP and USMA to define evidence needs and integrate the strategy for launch and lifecycle.
  • Design and execute HEOR studies (e.g., network meta-analyses; real-world evidence/non-interventional studies), including site engagement, chart abstraction, and retrospective data collection, from concept through publication.
  • Develop US value & evidence strategy with US Medical and Global HV&E, including AMCP dossiers, systematic literature reviews, economic models, and tools to support reimbursement and access.
  • Provide strategic input into clinical trial designs and PRO data analysis/interpretation to support reimbursement, differentiation negotiations, and patient access.
  • Ensure appropriate dissemination of HEOR materials per regulatory guidance/internal SOPs (e.g., PVPs, promotional materials, FDAMA 114-compliant materials).
  • Build external research collaborations with experts, healthcare policy makers, payers, and academic/community oncology settings.
Qualifications:
  • Graduate degree minimum (e.g., MSc/MPH/PhD) required.
  • 7+ years with MSc/MPH/MBA; or 5+ years with PharmD/PhD in HEOR or related fields.
  • Deep understanding of health services research methods (health economic modeling, PROs, statistics, real-world evidence/registries/observational design) and independent management of complex non-interventional studies.
  • Knowledge of drug development and US healthcare/economic environment.
Preferred Qualifications:
  • Experience managing real-world evidence studies (sites, chart abstraction vendors, data quality oversight, protocol-aligned abstraction).
  • Oncology/lung cancer experience.
  • Experience with US healthcare environment and HTA submissions (e.g., ICER, CMS-IPAY/IRA, NICE).
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