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22 часа назад

Executive Director, Head of Clinical Supply Planning and Operations SCM

255 000 - 425 000$
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, Head of Clinical Supply Planning and Operations SCM (Clinical Supply Operations): Leading global clinical supply operations for oncology and specialty medicine drug candidates from early development through launch and lifecycle management with an accent on clinical trial materials, comparator management, vendors, and supply chain governance. Focus on coordinating complex cross-functional programs across the US, Japan, and EU, managing global CSO organizations, and ensuring compliant, reliable supply for clinical development.

Location: Basking Ridge, New Jersey, United States; travel up to 20% domestically and internationally, including Japan, Germany, and China.

Salary: USD 255,000–425,000 per year

Company

hirify.global is a global healthcare company developing innovative medicines in oncology, cardiovascular disease, rare diseases, and immune disorders.

What you will do

  • Lead the global Clinical Supply Operations strategy for oncology and specialty medicine programs from early development through launch and lifecycle management.
  • Oversee clinical trial materials, comparator management, packaging, labeling, inventory, logistics, storage, distribution, transfer, and destruction.
  • Manage CSO functions across hirify.global entities and coordinate delivery of clinical supplies for global development projects.
  • Establish governance and oversight for clinical supply vendors, including Interactive Response Technology, labeling, distribution, and storage providers.
  • Represent Clinical Supply Operations in supply chain committees, steering committees, and collaboration governance with AstraZeneca and Merck Sharp & Dohme.
  • Lead organizational change, workforce development, budgeting, resource planning, and cross-functional collaboration with R&D, clinical, quality, regulatory, finance, and supply chain stakeholders.

Requirements

  • Bachelor’s degree in a scientific or technical discipline is required.
  • At least 15 years of relevant biotechnology or pharmaceutical industry experience.
  • At least 12 years of experience in Clinical Supply Operations or a related pharmaceutical development field with global scope.
  • Extensive experience in oncology project development and cold chain management.
  • Experience managing cross-functional teams in a matrix organization.
  • Ability to travel up to 20% of the time, including domestic and international travel.

Nice to have

  • Master’s degree in chemistry, life sciences, engineering, pharmaceutical sciences, or a related discipline.
  • PhD in a relevant scientific or technical field.

Culture & Benefits

  • Work within a global organization with more than 30 countries of presence and over 19,000 employees.
  • Collaborate with stakeholders across the US, Japan, and EU.
  • Contribute to the company’s 2030 vision and organizational transformation.
  • Equal opportunity and affirmative action employment environment.

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