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8 дней назад

Director, Clinical Supply Chain Operations (Biotech)

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
Director, Clinical Supply Chain Operations (Biotech): Developing and managing global clinical supply strategies covering demand planning, packaging, labeling, distribution, logistics, and vendor operations with an accent on clinical trial supply continuity, regulatory readiness, and cross-functional execution. Focus on designing contingency plans, managing global inventory and import/export logistics, leading supplier governance, and driving digital transformation with forecasting tools and AI-driven analytics.

Location: Hybrid role based out of the Bridgewater, New Jersey office, with remote work available most of the time and in-person collaboration as needed. Occasional domestic and international travel of approximately 25% is required.

Company

hirify.global is a global biopharmaceutical company developing treatments for patients with serious and rare diseases.

What you will do

  • Develop and execute global clinical supply strategies, including demand and production planning, packaging, labeling, distribution, returns, reconciliation, destruction, and logistics.
  • Define sourcing strategies and manage relationships with CMOs, CROs, 3PLs, IXRS/IRT vendors, and other external providers.
  • Establish KPIs, scorecards, governance frameworks, budgets, forecasts, and supplier performance reviews.
  • Translate clinical protocols into supply plans, contingency strategies, and risk mitigation across global markets.
  • Lead and mentor Clinical Supply managers, build high-performing cross-functional teams, and collaborate with Clinical Operations, CMC, Quality, Regulatory, and Commercial Supply.
  • Oversee depot inventory, labeling, temperature excursions, import/export logistics, supply tracking, audit readiness, and patient supply continuity.

Requirements

  • Bachelor’s degree in science, business, or a related field.
  • 10+ years of experience leading clinical supply chain and logistics activities.
  • Extensive experience planning and executing investigational materials supply strategies.
  • Expert knowledge of drug development phases, biopharmaceutical processes, and project management principles.
  • Experience working across Clinical, Regulatory, and Quality functions in a highly matrixed environment.
  • Ability to lead teams, manage cross-functional resources, support regulatory filings, and maintain inspection and audit readiness.

Nice to have

  • Master’s degree or MBA.
  • Experience in drug development.

Culture & Benefits

  • Flexible work schedules with purposeful in-person collaboration.
  • Medical, dental, vision, and mental health coverage.
  • Paid time off, fertility and family-forming benefits, and caregiver support.
  • 401(k) plan with company match, equity awards, ESPP, and company-paid life and disability insurance.
  • Learning programs, mentorship, employee resource groups, and service opportunities.

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