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9 дней назад

Associate Director, Clinical Supply Chain (Oncology)

167 000 - 206 000$
Формат работы
onsite
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
Associate Director, Clinical Supply Chain (Oncology): Managing clinical trial materials for global oncology studies with an accent on demand forecasting, inventory management, packaging, labeling, distribution, and vendor oversight. Focus on coordinating IRT systems, supporting compliant international shipments, and mitigating supply risks across phase 1–3 clinical trials.

Location: South San Francisco, California, United States; onsite at the headquarters four days per week. Travel is required for 5–10% of the year, domestically.

Salary: $167,000–$206,000 annually

Company

hirify.global is a precision medicine oncology company developing targeted therapies, including small-molecule treatments and antibody-drug conjugates for genetically defined solid tumors.

What you will do

  • Manage clinical trial material planning, forecasting, inventory, sourcing, packaging, labeling, distribution, returns, and destruction.
  • Coordinate clinical supply requirements with Clinical Operations, CMC, QA, QC, Regulatory, Clinical Development, and Program Management.
  • Manage external depots, couriers, contract packaging organizations, CROs, and other clinical supply vendors.
  • Develop and maintain study-specific supply plans, pharmacy manuals, training materials, and Trial Master File documentation.
  • Manage IRT specifications, user acceptance testing, inventory monitoring, resupply, system updates, and supply-related issue resolution.
  • Oversee global CTM shipment documentation, customs clearance support, labeling releases, expiry extensions, and compliant delivery to clinical sites.

Requirements

  • Bachelor’s degree in Supply Chain, Engineering, life sciences, or a related field.
  • 10+ years of experience in the biotechnology or pharmaceutical industry, including 7+ years in supply chain.
  • Experience with clinical drug supply for global phase 1–3 trials, Expanded Access Programs, and investigator-sponsored trials.
  • Demonstrated expertise in forecasting, inventory management, drug allocation, IRT systems, packaging, labeling, and international shipment processes.
  • Knowledge of GMP, GDP, GCP, regulatory timing, global distribution, and logistics.
  • Ability to work cross-functionally, anticipate supply risks, and develop mitigation strategies.

Nice to have

  • Experience with CMC operations and drug supply forecasting technology.
  • APICS, CPIM, CIRM, or PMP certification.

Culture & Benefits

  • Collaborative, inclusive, and data-driven environment focused on advancing precision oncology therapies.
  • Medical, dental, and vision coverage, with the company paying 100% of employee premiums and 90% of dependent premiums.
  • 401(k), employee stock purchase plan, wellness programs, and potential merit-based increases.
  • Eligibility for discretionary short-term incentives and stock option awards.

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