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2 дня назад

Executive Director, Global Program Leader (in vivo CAR-T)

256 073 - 336 097$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
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
Executive Director, Global Program Leader (in vivo CAR-T): Leading global development and governance of in vivo CAR-T programs from IND-enabling studies through clinical proof-of-concept, registration, and lifecycle management with an accent on integrated scientific, clinical, regulatory, manufacturing, and commercial strategy. Focus on chairing cross-functional global program teams, guiding regulatory submissions and health authority interactions, and managing portfolio decisions, risks, milestones, and investment priorities.

Location: Hybrid role based in Somerset, New Jersey, United States. Applicants must be authorized to work in the United States.

Base pay: $256,073–$336,097 USD per year, plus performance-based bonus and/or equity for eligible roles.

Company

hirify.global is a biotechnology company developing cell and gene therapies, including CAR-T, TCR-T, and natural killer cell-based therapies, in collaboration with global partners.

What you will do

  • Lead the strategy, execution, governance, and development lifecycle of assigned in vivo CAR-T programs.
  • Build integrated global development plans covering scientific, clinical, regulatory, manufacturing, commercial, resource, budget, and milestone objectives.
  • Chair Global Program Teams and coordinate Research, Clinical Development, Regulatory Affairs, Translational Sciences, CMC, Manufacturing, Quality, Commercial, Finance, and Business Development.
  • Lead global clinical development, registration, IND, CTA, BLA/MAA, and lifecycle management strategies.
  • Drive portfolio decisions, investment analyses, risk management, contingency planning, and resolution of strategic and operational issues.
  • Present program strategies and recommendations to executive leadership, governance committees, external partners, investigators, and other stakeholders.

Requirements

  • 10+ years of biotechnology or pharmaceutical industry experience in drug development.
  • 5+ years of leadership experience managing complex, global development programs.
  • Proven success advancing biologics, cell therapies, gene therapies, or other advanced therapeutic programs through clinical development.
  • Experience leading cross-functional development teams in a matrix environment and supporting global regulatory interactions and major submissions.
  • Deep knowledge of global drug development, clinical development, registration pathways, and cell and gene therapy technologies, including emerging in vivo CAR-T approaches.
  • Strong strategic thinking, portfolio management, executive communication, financial awareness, risk management, and global team leadership skills.

Nice to have

  • Experience in oncology, immunology, cell therapy, gene therapy, or in vivo genetic medicines.

Culture & Benefits

  • Permanent full-time employees receive medical, dental, and vision insurance and a 401(k) plan with company match fully vested on day one.
  • Benefits include eight weeks of paid parental leave after three months, paid vacation and sick time, floating holidays, and eleven company holidays.
  • Additional benefits include flexible spending and health savings accounts, disability coverage, life insurance, legal assistance, commuter benefits, and family care resources.
  • Performance-based bonus and/or equity is available for eligible roles.

Hiring process

  • Selected candidates must complete Form I-9 employment verification through the E-Verify program.

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