Clinical Supplies Manager

Drive global clinical supply strategies that ensure investigational products reach patients reliably and on time. This role partners across development, quality, operations, and external vendors to support a diverse clinical portfolio with precision and agility.

Responsibilities

• Develop and communicate supply strategies for assigned studies.
• Collaborate with cross‑functional teams to align timelines, forecasts, and regulatory needs.
• Review protocols and influence study design from a supply perspective.
• Build and manage supply forecasts; monitor inventory and country‑specific requirements.
• Initiate manufacturing, packaging, and labelling activities.
• Oversee distribution planning, IRT setup, and depot/site supply strategies.
• Support use‑date extensions, inspection readiness, deviations, and change controls.
• Serve as primary supply contact for assigned compounds.
• Contribute to sourcing of commercial comparators and maintain study budgets.
• Drive continuous improvement across clinical supply processes.

Requirements

• Experience in pharma with a focus on clinical supplies or clinical development.
• Strong understanding of global development processes and regulatory expectations.
• Proficiency in forecasting, planning, logistics, packaging/labelling, and IRT systems.
• Strong analytical, communication, negotiation, and project management skills.
• Ability to influence teams, resolve conflicts, and translate strategy into action.
• Leadership experience and ability to mentor or guide others.

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