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Cogent Biosciences

Develops small-molecule therapies for rare diseases

Senior Director - Global Market Access

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWaltham, MA, USA

About the Job

Requirements

  • A bachelor's degree in a relevant discipline is required; an advanced degree such as an MBA, MPH, PharmD, or MS is preferred.
  • At least 10 years of experience in pharmaceutical or biotechnology market access, pricing, reimbursement, health economics and outcomes research (HEOR), or a related discipline.
  • Demonstrated experience developing market access strategies in the United States and international markets.
  • Experience in oncology, specialty pharmaceuticals, or other complex therapeutic areas.
  • Experience supporting products through development and/or commercialization, ideally including a launch.
  • Experience translating clinical evidence and product value into payer and health technology assessment (HTA) strategies.
  • Understanding of global pricing, reimbursement, and HTA environments.
  • Strong analytical, strategic planning, project management, and communication skills.

Responsibilities

  • Develop and execute global market access strategies for oncology pipeline and commercial products across the product lifecycle.
  • Identify market access opportunities, risks, and potential barriers across the United States and priority international markets.
  • Develop market-specific strategies informed by payer dynamics, reimbursement and HTA requirements, clinical practice, treatment pathways, and competitive landscapes.
  • Integrate market access, pricing, reimbursement, HEOR, and value considerations into broader product, development, and commercialization strategies.
  • Monitor changes in oncology treatment, reimbursement, and health-system environments and assess implications for the portfolio.
  • Lead the integration of market access and HEOR perspectives into the overall value strategy for oncology assets.
  • Translate the clinical profile, unmet need, and treatment landscape into differentiated payer and HTA value propositions.
  • Partner with HEOR and Medical Affairs to define evidence requirements and develop evidence-generation strategies across key markets.
  • Provide market access input into clinical development plans, endpoints, comparators, patient populations, and evidence-generation priorities.
  • Identify evidence gaps that may create future access barriers and work with HEOR and cross-functional teams to address them.
  • Guide development of value dossiers, economic models, budget impact analyses, and other market access tools in partnership with HEOR.
  • Ensure HEOR outputs are effectively translated into payer, HTA, and broader market access strategies.
  • Develop and support global pricing and reimbursement strategies with the VP, Value & Access Strategy, and cross-functional stakeholders.
  • Conduct pricing and reimbursement assessments across priority markets, considering clinical value, treatment alternatives, healthcare-system dynamics, and market access requirements.
  • Develop pricing scenarios and assumptions to support business planning, forecasting, and strategic decision-making.
  • Ensure pricing considerations are integrated with the overall value and access strategy throughout the product lifecycle.
  • Serve as a core market access leader within cross-functional launch teams.
  • Develop market access launch plans, milestones, risks, and mitigation strategies.
  • Incorporate payer, reimbursement, pricing, HTA, and evidence considerations into launch sequencing and commercialization planning.
  • Support development of payer-facing materials and value communication tools.
  • Help establish appropriate access metrics and readiness assessments.
  • Ensure the organization is prepared to address market access considerations in key launch markets.

About the Company

Cogent Biosciences

Develops small-molecule therapies for rare diseases

Cogent Biosciences develops small molecule therapies for rare, genetically driven diseases. Its work centers on discovering and advancing compounds that can address conditions with limited treatment options, using a research-driven approach to guide drug discovery and development through clinical trials. The lead candidate, CGT9486, is progressing in three clinical trials planned for this year, alongside ongoing work in collaboration with partners. The company differentiates itself through its focus on genetically defined diseases, its emphasis on targeted small molecules, and its strategy of advancing candidates via internal science and partnerships, supported by a strong financial position that includes a cash reserve of $242.2 million. Cogent’s goal is to bring effective therapies to patients with unmet needs by progressing its drug candidates toward potential commercialization and forming strategic collaborations to maximize development and access.

Company size
201-500
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2014

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