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10 дней назад

Clinical Supply Chain Project Leader (AI)

Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
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
Clinical Supply Chain Project Leader (AI): Defining and implementing clinical supply chain strategies for pharmaceutical development projects with an accent on IMP supply, study oversight, timelines, quality, and budget. Focus on leading cross-functional stakeholders, managing GCP/GMP compliance and supply risks, and driving process improvements through digital tools and forecasting systems.

Location: Cambridge, Massachusetts, United States; hybrid work

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines through immunoscience, data, and digital technologies.

What you will do

  • Define and implement clinical supply chain strategies aligned with project objectives, KPIs, timelines, quality, and budget.
  • Assess study design feasibility and optimize labeling, packaging, outsourcing, distribution, and IMP supply decisions.
  • Lead Clinical Supply Chain Study Leaders and oversee operational activities across multiple clinical trials.
  • Monitor plan execution, costs, lead times, quality, risks, and mitigation actions using KPIs and digital tools.
  • Represent clinical supply chain in project meetings and coordinate with GPH, CMC, clinical leaders, contractors, and other stakeholders.
  • Drive process improvement, knowledge sharing, and preparation for PAI activities.

Requirements

  • Bachelor’s degree with at least 5 years of experience, or a master’s degree with at least 3 years of experience, preferably in health sciences, engineering, pharmacy, chemistry, biology, or a related discipline.
  • Experience in the pharmaceutical industry, preferably in clinical supply chain, clinical operations, or manufacturing.
  • Project management experience with strong leadership, organizational, prioritization, communication, negotiation, and influencing skills.
  • Experience working across functions and cultures in complex, matrixed organizations.
  • Knowledge of GxP regulations and IMP requirements.
  • Ability to manage risks, solve problems, make decisions, and maintain effective stakeholder relationships.

Nice to have

  • Experience with N-SIDE forecasting systems or IRT systems.
  • Risk management experience.

Culture & Benefits

  • Supportive, future-focused environment with opportunities for promotion and international career moves.
  • Health and wellbeing benefits, including healthcare, prevention, and wellness programs.
  • At least 14 weeks of gender-neutral parental leave.
  • Work involving AI, data, and digital platforms at the forefront of drug discovery.
  • Opportunity to contribute to faster, more effective drug development and patient-focused study design.

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