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6 дней назад

VP, DM1 Commercial Asset Lead (Biotech)

272 000 - 340 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
head
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
VP, DM1 Commercial Asset Lead (Biotech): Defining and executing the global commercialization strategy and launch readiness for Dyne’s DM1 therapeutic asset with an accent on competitive positioning, market access, reimbursement, and cross-functional program integration. Focus on leading global launches starting with the U.S., aligning affiliate teams, and advancing the asset from late-stage development through approval and launch.

Location: Onsite in Waltham, Massachusetts, United States

Salary: $272,000–$340,000 USD base pay annually

Company

hirify.global is a clinical-stage biotechnology company developing oligonucleotide therapeutics for genetically driven neuromuscular diseases.

What you will do

  • Define the global commercialization strategy and execution plan for the DM1 asset.
  • Lead launch planning and readiness across key markets, starting with the United States.
  • Shape competitive positioning, product differentiation, value proposition, label strategy, and access planning.
  • Lead the DM1 Commercial Sub-Team and drive cross-functional decisions across medical, regulatory, supply, marketing, digital, and data functions.
  • Partner with affiliate teams and external stakeholders to support reimbursement and market access readiness.
  • Engage with key opinion leaders, patient advocacy groups, care teams, payers, regulators, and senior leadership.

Requirements

  • Bachelor’s degree in a relevant scientific, medical, or business discipline; an advanced degree is strongly preferred.
  • Minimum of 20 years of experience in the biopharmaceutical industry.
  • At least 15 years of commercialization and cross-functional leadership experience.
  • Extensive global product launch experience, including at least three launches.
  • Experience steering assets from late-stage development through approval and launch, including global and U.S. market access and reimbursement readiness.
  • Onsite work in Waltham, Massachusetts, United States is required.

Nice to have

  • Rare disease experience.
  • Neuromuscular disease experience.

Culture & Benefits

  • Patient-centric work focused on functional improvement for people living with genetically driven diseases.
  • Collaboration across clinical, medical, regulatory, supply, and commercial functions.
  • Opportunity to contribute to a broad neuromuscular disease pipeline and global launch programs.

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