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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Director – Global Value & Access Strategy - Endocrinology

Product MarketingConfirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • At least 8 years of direct biotechnology or pharmaceutical industry experience and/or payer experience.
  • Deep working knowledge of United States and ex-United States healthcare systems.
  • Experience leading cross-functional teams.
  • Ability to think strategically and make sound pricing and market access recommendations.
  • Strong practical, quantitative, and analytical skills, with an understanding of applying pricing, reimbursement, and health economics and outcomes research (HEOR) principles.
  • General experience in commercialization and drug development.
  • Outstanding written and oral communication skills, including the ability to write and deliver presentations to professionals at all levels within the organization.
  • Demonstrated relationship-building at all organizational levels and across geographies.
  • A Bachelor of Arts or Bachelor of Science in a field of study requiring quantitative analysis.

Responsibilities

  • Develop global payer strategic plans to support value and access optimization for atumelnant as a potential first-in-class therapy for congenital adrenal hyperplasia.
  • Partner cross-functionally and across regions to develop global commercial strategic recommendations with aligned commercial input.
  • Develop global pricing and market access strategy and pricing policy for the potential global launch of atumelnant in congenital adrenal hyperplasia.
  • Develop compliant strategies to enable global patient access to atumelnant before formal reimbursement agreements conclude, where permitted.
  • Lead cross-functional initiatives to secure timely payer scientific advice in key global geographies and inform payer evidence-generation planning.
  • Provide access input to atumelnant global evidence-generation strategies with cross-functional partners to optimize global access.
  • Develop and roll out a global unbranded payer message platform to support payer disease awareness and market development in congenital adrenal hyperplasia.
  • Develop payer value communication materials for atumelnant, including a branded payer value narrative, rollout and training, price messaging, and a pricing objection handler.
  • Ensure atumelnant lifecycle-management initiatives and potential future indications are optimized for access.
  • Represent Global Value & Access Strategy and embed the global payer perspective in relevant cross-functional atumelnant operating teams and workstreams.
  • Support pricing and market access capability-building and thought-leadership projects that advance knowledge of and readiness for the evolving global payer environment.
  • Monitor market trends, competition, product acceptance, and new product releases, and adjust Market Access plans accordingly.
  • Support global commercialization efforts and reimbursement negotiations for Palsonify, including negotiation strategy, financial considerations, and identification and prioritization of evidence needed to sustain value over time.
  • Support global pricing and market access governance, including input to price policy, governance framework, and negotiation business cases.
  • Ensure the payer perspective is embedded in ongoing Palsonify lifecycle-management initiatives, including input into development strategy, evidence generation, and commercialization priorities.

Desired Qualifications

  • Experience in specialty and/or rare disease access models.
  • Experience in a comparable global role.
  • An advanced degree.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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