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3 часа назад

Clinical Supply Chain Project Leader (Biopharma)

105 000 - 151 666$
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 (Biopharma): Defining and implementing clinical supply chain strategies for clinical development projects with an accent on IMP supply, study oversight, quality, timelines, and budget. Focus on coordinating multiple trials, monitoring risks and KPIs, reducing lead times and costs, and aligning cross-functional stakeholders under GCP/GMP requirements.

Location: Cambridge, MA, United States; hybrid work

Salary: $105,000–$151,666.66 per year

Company

R&D-driven, AI-powered biopharma focused on 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 influence labeling, packaging outsourcing, and distribution network decisions.
  • Lead Clinical Supply Chain Study Leaders and oversee operational activities across multiple clinical trials.
  • Monitor execution, costs, lead times, quality, and risks; implement mitigation and process improvement plans.
  • Represent Clinical Supply Chain in project decisions and coordinate with GPH, CMC, and Clinical leaders.
  • Escalate IMP, device, AxMP, and comparator issues; report progress and facilitate stakeholder communication.

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, organization, prioritization, communication, negotiation, and influencing skills.
  • Ability to collaborate across functions and operate effectively in cross-cultural, complex organizational matrices.
  • Experience with GxP regulations and IMP requirements is preferred.

Nice to have

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

Culture & Benefits

  • Supportive, future-focused environment centered on scientific innovation and patient impact.
  • Career growth opportunities through promotions and lateral moves, including international opportunities.
  • Rewards package recognizing employee contributions.
  • Healthcare, prevention, wellness, and family benefits, including at least 14 weeks of gender-neutral parental leave.
  • Work at the forefront of drug discovery using AI, data, and digital platforms.

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