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BeOne

Global oncology therapeutics discovery, development, manufacturing

Director – Value Demonstration & Access Evidence Strategy - Hematology

Biology & BiotechConfirmed live in the last 24 hours
Full-timeBasel, SwitzerlandCHF198.2k - CHF247.7k

About the Job

Requirements

  • An MSc, MPH, or equivalent advanced degree in health economics, epidemiology, public health, biostatistics, life sciences, or health policy is required.
  • At least 8 years of experience in market access, health economics and outcomes research, value and access, or evidence strategy is required.
  • Demonstrated experience supporting health technology assessment submissions, reimbursement negotiations, evidence planning, and global launch preparation is required.
  • Strong understanding of EU health technology assessment and Joint Clinical Assessment, real-world evidence methodologies, economic modelling, clinical development, and international payer decision-making is required.
  • Ability to lead cross-functional and cross-regional initiatives and influence without direct authority in a matrixed global organization is required.
  • Excellent written and verbal communication skills in English are required.
  • Regular scheduled engagement with U.S.-based Value & Access, health economics and outcomes research, and Medical colleagues is required.
  • Sufficient working-hour overlap with both U.S. Eastern and Central European time zones is required.
  • International travel is expected to support cross-functional and regional collaboration; travel is 15% of the time.

Responsibilities

  • Design and implement global health technology assessment and payer evidence strategies across the product lifecycle.
  • Work with Global Value, Access & Pricing asset leads, regional and country access leads, and health economics and outcomes research teams to identify evidence requirements supporting Joint Scientific Consultations, Joint Clinical Assessments, national health technology assessments, reimbursement submissions, and pricing negotiations.
  • Evaluate evidence-option trade-offs and recommend risk-mitigation strategies that optimize payer, access, pricing, and development objectives.
  • Ensure access evidence requirements are embedded in Integrated Evidence Plans.
  • Provide market-access and health technology assessment input into clinical development programmes, registrational study design, comparator strategy, endpoint selection, patient-population selection, subgroup evidence generation, patient-reported outcome strategy, and real-world evidence generation.
  • Influence development decisions to address future reimbursement risks proactively.
  • Serve as the standing point of contact for U.S. Value & Access, U.S. health economics and outcomes research, and U.S. Medical teams on pipeline evidence planning.
  • Elicit, document, and prioritize U.S. payer, pharmacy benefit manager, integrated delivery network, and employer evidence requirements, including comparator expectations, endpoint and subgroup needs, real-world data requirements, AMCP-format dossier inputs, and Institute for Clinical and Economic Review assessment risk; ensure these requirements are represented alongside EU health technology assessment and other non-U.S. requirements in Integrated Evidence Plans.
  • Identify and escalate conflicts between U.S. and non-U.S. evidence requirements, recommend resolutions, and articulate trade-offs.
  • Anticipate access implications of U.S. policy developments, including Centers for Medicare & Medicaid Services price negotiation and Medicare/Medicaid coverage dynamics, and translate them into evidence-generation requirements while development decisions remain open.
  • Develop and maintain asset-specific payer value-demonstration plans.
  • Shape evidence-generation activities with health economics and outcomes research, including cost-effectiveness analyses, budget-impact models, real-world evidence studies, patient-reported outcome studies, long-term outcome analyses, indirect treatment comparisons, and network meta-analyses.
  • Collaborate with health economics and outcomes research and Medical Affairs teams to ensure evidence packages address stakeholders across global healthcare systems.
  • Monitor evolving global health technology assessment methodologies and payer evidence expectations, including EU HTA Regulation, NICE, HAS, G-BA/IQWiG, AIFA, CADTH, ICER, and other major payer and assessment bodies, and translate developments into concrete evidence requirements for U.S.-relevant programmes.
  • Translate emerging requirements into actionable evidence-generation strategies.
  • Prepare assets for EU-level and local health technology assessment decision-making.
  • Support Global Value, Access & Pricing asset leads in developing payer-focused value propositions.
  • Translate clinical, economic, and patient-centered evidence into core value narratives, health technology assessment dossiers, global value dossiers, pricing toolkits, and reimbursement materials.
  • Provide expert input into key messages and evidence-based value stories for payer and health technology assessment engagement.
  • Build and maintain relationships with health technology assessment experts, policy experts, and academic researchers.
  • Represent the organization in scientific and methodological discussions.
  • Contribute to the advancement of access-related methodologies and evidence-generation best practices.
  • Contribute to capability building and continuous improvement across Global Value, Access & Pricing.

Desired Qualifications

  • A PhD, PharmD, or MD is preferred.
  • Additional business or strategic leadership education is preferred.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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