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7 дней назад

Drug Supply Manager (Pharmaceutical)

Формат работы
onsite
Тип работы
fulltime
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
Drug Supply Manager (Pharmaceutical) (Clinical Supply Chain): Developing strategic clinical drug supply plans, demand forecasts, budgets, and distribution schedules for R&D programs with an accent on manufacturing, packaging, labeling, and depot delivery. Focus on coordinating CROs and CMOs, managing supply risks, supporting regulatory filings, and improving end-to-end clinical supply processes.

Location: Princeton, NJ, United States

Company

Big pharmaceutical organisation.

What you will do

  • Provide strategic direction for end-to-end clinical drug supply chain planning across assigned R&D programs.
  • Develop program-level demand forecasts, supply plans, cost estimates, and budgets for clinical drug substance, drug product, packaging, labeling, release, and depot delivery.
  • Review study-level demand projections, adjust supply plans and budgets, and influence manufacturing and purchasing priorities.
  • Coordinate with clinical, manufacturing, procurement, packaging, labeling, logistics, IRT, regulatory, and data management teams to meet study timelines.
  • Serve as the primary drug supply liaison for CROs, CMOs, sourcing vendors, and strategic alliance partners, including support for clinical supply agreements.
  • Manage supply-related quality events, field complaints, CAPAs, product information listings, batch extract files, and process improvement initiatives.

Requirements

  • Experience planning and managing clinical drug supply across clinical development programs.
  • Ability to create demand forecasts, supply plans, budgets, cost estimates, and manufacturing or purchasing requirements.
  • Experience coordinating cross-functional teams and external CRO, CMO, and vendor partners.
  • Understanding of clinical study implementation, packaging and labeling, IRT setup, regulatory documentation, and drug supply timelines.
  • Ability to identify supply risks, communicate with stakeholders, and escalate issues appropriately.
  • Ability to work from the Princeton, New Jersey location.

Culture & Benefits

  • Full-time employment within a large pharmaceutical organisation.
  • Cross-functional collaboration across clinical supply, operations, development, regulatory, logistics, and data teams.
  • Matrix collaboration with Drug Planning Coordinators and Specialists, with no direct reports.
  • Opportunities to lead task forces and improve clinical supply procedures and efficiency.

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