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Director, Clinical Supply Chain Operations (Biopharmaceutical)

177 000 - 242 000$
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 (Biopharmaceutical): Leading global clinical supply chain operations for investigational materials, including demand planning, production, packaging, distribution, logistics, and budgeting with an accent on supplier governance, regulatory readiness, and patient supply continuity. Focus on designing global supply strategies, managing inventory and risks, coordinating cross-functional clinical programs, and driving digital transformation through forecasting tools, dashboards, and AI-driven analytics.

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

Salary: $177,000–$242,000 annual.

Company

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

What you will do

  • Lead global demand planning and execution of clinical supply activities across production, packaging, labeling, distribution, returns, reconciliation, destruction, and logistics.
  • Develop sourcing strategies and manage relationships with CMOs, CROs, 3PLs, IXRS/IRT vendors, and other external providers.
  • Establish KPIs, scorecards, governance frameworks, vendor reviews, and continuous improvement processes.
  • Translate clinical protocols into supply plans, contingency strategies, budgets, forecasts, and risk-mitigation actions.
  • Oversee depot inventory, labeling strategies, temperature excursions, import/export logistics, regulatory documentation, audit readiness, and patient supply continuity.
  • Lead team development and collaborate with Clinical Operations, CMC, Quality, Regulatory, Commercial Supply, and digital transformation teams.

Requirements

  • Bachelor’s degree in a science or business-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 applicable project management principles.
  • Experience working across Clinical, Regulatory, and Quality functions in a highly matrixed environment.
  • Ability to build high-performing teams, integrate cross-functional resources, and lead managers or direct reports.

Nice to have

  • Master’s degree or MBA.
  • Development experience.

Culture & Benefits

  • Medical, dental, vision, and mental health coverage.
  • Annual wellbeing reimbursement and Employee Assistance Program access.
  • Paid time off, family-forming benefits, caregiver support, and flexible work schedules.
  • 401(k) with company match, annual equity awards, ESPP, and company-paid life and disability insurance.
  • Learning programs, mentorship, employee resource groups, service programs, and recognition initiatives.

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