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6 дней назад

Senior Manager, Clinical Supply Integration (Oncology)

150 000 - 160 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Senior Manager, Clinical Supply Integration (Oncology): Coordinating the end-to-end flow of investigational medicinal products across manufacturing, packaging and labeling, release, logistics, depots, and clinical sites with an accent on global clinical supply execution, vendor coordination, and timeline management. Focus on managing complex dependencies, identifying and resolving operational risks, and scaling supply operations across late-stage oncology programs.

Location: Based out of the San Francisco or Boston office; requires 10–15% domestic or international travel.

Base pay: $150,000–$160,000 annually, plus equity, bonus, and benefits.

Company

hirify.global is a clinical-stage biopharmaceutical company developing therapies for breast cancer and other metastatic cancers, including palazestrant and OP-3136.

What you will do

  • Coordinate end-to-end clinical supply activities across global CDMOs in the US, EU, UK, APAC, and LATAM.
  • Oversee packaging, labeling, procurement, manufacturing runs, QP release, logistics, distribution, clinical depots, and trial-site supply.
  • Align Clinical Supply, Clinical Operations, Quality, Regulatory, CMC, Finance, and external vendors.
  • Maintain supply timelines, protocols, procedures, systems, and documentation for clinical programs.
  • Support departmental budgets, monitor project progress, and escalate risks and issues through resolution.
  • Drive continuous improvement through SOPs, lessons learned, best practices, and operational scaling.

Requirements

  • Bachelor’s degree required; master’s degree preferred.
  • 8+ years of progressive clinical supply experience with a bachelor’s degree, or 6+ years with a master’s degree, in biotechnology or pharmaceuticals.
  • Strong understanding of global clinical supply operations and working knowledge of GMP, GDP, Quality, Clinical Operations, and regulatory requirements.
  • Experience coordinating manufacturing, packaging and labeling, release, inventory, demand, expiry, logistics, and distribution activities.
  • Strong project management, data reconciliation, vendor management, governance, analytical judgment, and risk-management skills.
  • Ability to manage complex timelines and dependencies while influencing cross-functional partners without direct authority.

Nice to have

  • Experience supporting complex global or late-stage clinical studies.
  • Oncology clinical trial experience.
  • Master’s degree.

Culture & Benefits

  • Collaborative, pragmatic, agile, and operationally focused working environment.
  • Commitment to patients, quality, teamwork, continuous improvement, and operational excellence.
  • Competitive compensation and benefits package including equity and bonus.
  • Open, flexible, and friendly environment supporting long-term career development.

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