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Stoke Therapeutics

Develops targeted gene upregulation therapies

Regional Medical Director - Value and Access, East

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • An advanced clinical or scientific degree in a relevant discipline is required.
  • At least 10 years of progressive experience in Medical Affairs, payer medical engagement, Market Access, HEOR/RWE, clinical development, managed care, or a related pharmaceutical or biotechnology function is required.
  • Deep expertise in managed care, formulary and coverage decision-making, evidence-based medicine, clinical trial methodology, health economics and outcomes research, outcomes research, epidemiology, and real-world evidence is required.
  • Ability to connect external stakeholder needs with portfolio, evidence-generation, access, and medical priorities is required.
  • Executive-level scientific communication, facilitation, and presentation skills are required.
  • Ability to critically appraise complex clinical and economic data, identify limitations, and articulate implications for population-health decisions is required.
  • Business and financial acumen, including prioritization, resource allocation, project planning, and measurement of impact, is required.
  • Ability to influence in matrixed organizations and lead across functions, geographies, and levels without direct authority is required.
  • Sound judgment in ambiguous, high-visibility, and compliance-sensitive situations is required.
  • Coaching, mentoring, change leadership, and capability-building skills are required.
  • Ability to use digital engagement, insight analytics, and customer relationship tools effectively is required.
  • Must reside within or have practical access to the assigned region and be able to travel overnight as business needs require.
  • Must complete required training and reporting accurately and on time.

Responsibilities

  • Develop and execute a regional stakeholder engagement plan aligned with medical, evidence, and corporate priorities.
  • Build peer-to-peer scientific relationships with senior clinical and population-health leaders across national and regional health plans, pharmacy benefit managers, Medicaid organizations, integrated delivery networks, accountable care organizations, employer coalitions, and health technology assessment bodies.
  • Serve as the senior scientific contact for complex payer and reimbursement questions, including pre-launch and launch engagements.
  • Lead balanced, non-promotional exchange on disease state, clinical data, guidelines, safety and efficacy, comparative evidence, health economics and outcomes research, real-world evidence, and pipeline information where appropriate.
  • Plan and run payer advisory boards and scientific forums, and ensure insights are captured and acted on.
  • Represent Medical Affairs at regional and national payer meetings and external forums.
  • Lead regional communication of the totality of evidence, including efficacy, safety, comparative data, health economics and outcomes research, quality of life, budget impact, epidemiology, and real-world evidence.
  • Develop and maintain payer-facing scientific materials and evidence summaries through appropriate review processes.
  • Translate complex evidence into clear, decision-relevant scientific narratives for sophisticated payer audiences.
  • Keep resources current, rigorous, and aligned with stakeholder needs.
  • Own the regional medical value plan and contribute to annual and lifecycle planning, prioritization, and resource allocation.
  • Gather and synthesize actionable insights on unmet needs, evidence expectations, coverage and policy changes, treatment paradigms, and competitive dynamics.
  • Escalate regional trends and strategic implications to Medical Affairs leadership and cross-functional governance.
  • Translate insights into recommendations for medical strategy, evidence generation, clinical development, publications, market access, and education.
  • Define and monitor regional Medical objectives, key performance indicators, and impact; adjust plans as needed.
  • Contribute senior scientific judgment to portfolio, indication, and lifecycle decisions while preserving Medical Affairs independence.
  • Provide regional leadership and strategic counsel across Medical Affairs, Field Market Access, health economics and outcomes research/real-world evidence, Clinical Development, Commercial within compliance guidelines, Government Affairs, Patient Services, Regulatory, Policy, and Medical Information.
  • Lead cross-functional workstreams for launch planning, payer evidence planning, advisory boards, congress strategy, and medical education.
  • Influence priorities and resolve competing needs without direct authority.
  • Inform regional resource allocation, manage assigned project budgets and external partners, and represent the regional perspective in US and global planning forums.
  • Identify and prioritize payer-relevant evidence gaps.
  • Partner with health economics and outcomes research/real-world evidence, Epidemiology, Clinical Development, and Market Access on evidence plans, research questions, endpoints, and dissemination.
  • Initiate or lead rigorous payer research collaborations, pragmatic pilots, data partnerships, investigator-sponsored research, and real-world evidence projects.
  • Provide senior field input into protocol concepts, publication strategy, congress communications, and medical information resources.
  • Evaluate emerging evidence and recommend changes to regional strategy and engagement.
  • Operate in accordance with applicable laws, industry codes, company policies, and standard operating procedures.
  • Maintain clear separation between scientific exchange and promotion, and apply sound judgment in novel situations.
  • Document and manage insights, engagements, research collaborations, materials, and transfers of value appropriately.
  • Identify operational risks, drive continuous improvement, and contribute to scalable field medical value processes.
  • Travel approximately 50–70% domestically to support priority regional and national payer engagements, medical meetings, and internal planning sessions.

Desired Qualifications

  • Formal training or demonstrated expertise in health economics, outcomes research, population health, managed care, epidemiology, or health policy is strongly preferred.

About the Company

Stoke Therapeutics

Develops targeted gene upregulation therapies

Stoke Therapeutics develops therapies for severe genetic diseases caused by loss of function in a single gene, aiming to restore missing proteins by upregulating protein expression. Its main product approach relies on the TANGO (Targeted Augmentation of Nuclear Gene Output) platform, which delivers precise, durable, and controllable upregulation of gene expression across a range of tissues to re-create the missing protein. Compared with many biotech firms, Stoke centers on upregulating endogenous gene output rather than replacing genes or adding new ones, and focuses on disease-modifying treatments for rare disorders with unmet medical needs. Revenue comes from partnerships, licensing agreements, and, ultimately, commercialization of its therapies. The company’s goal is to provide targeted, durable treatments that address the underlying genetic deficiency and improve outcomes for patients with limited options.

Company size
201-500
Company stage
IPO
Headquarters
Bedford, TX
Founded
2014

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