Clinical Supply Chain Project Leader
Listed on 2026-10-17
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Supply Chain/Logistics
Procurement / Purchasing, Operations Management, Regulatory Compliance Specialist
Job title
:
Clinical Supply Chain Project Leader
- Location:
Cambridge, MA
The Clinical Supply Chain Project Leader (CSC-PL) is accountable for IMP supply with respect to timelines, quality and budget for a given project.
The CSC-PL is responsible to:
- Defines and implements the CSC Strategy at project level.
- Oversees study management activities ensuring adherence to plan.
- Represents CSC at project level.
The CSC-PL will also ensure clear, concise, consistent, and timely communication with stakeholders and act as a change agent through the leadership of global initiatives targeting process improvement and engaging all partners throughout the clinical supply chain.
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.
About Sanofi:We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main responsibilities:CSC Strategy & Implementation
- Define and implement clinical supply chain strategy aligned with CSC KPIs and project objectives
- Assess study design feasibility ( card, Abbreviated Protocol stages) and optimize project delivery
- Influence Label & Pack outsourcing and distribution network strategy decisions
- Monitor supply chain performance (cost, lead times, quality) using KPIs and digital tools
- Drive continuous improvement and innovation across clinical supply chain operations
- Lead CSC-Study Leaders and oversee all operational activities ensuring compliance with GCP/GMP standards
- Ensure CSC strategy harmonization across multiple trials with adherence to timelines and budget
- Monitor plan execution, identify risks, and implement mitigation plans
- Identify opportunities to streamline processes and reduce lead times and costs
- Serve as primary point of contact for project team and coordinate PAI preparation
- Provide CSC expertise and contribute to project decision-making in project meetings.
- Escalate IMP/device/AxMP/comparator issues and propose mitigation strategies
- Interact with GPH, CMC leaders, and Clinical leaders to integrate CSC requirements into project strategy
- Report Progress and issues to CSC Leadership Team
- Facilitate knowledge sharing and provide feedback on contractor performance
Education:
- Bachelor’s degree with at least 5+ years OR Master’s degree with at least 3+ years preferably in Health Sciences or related disciplines (Engineering, Pharmacy, Chemistry, Biology, etc.)
Experience & Technical
Skills:
- Experience in pharmaceutical industry, preferably within clinical supply chain, clinical operations, or manufacturing environments.
- Project Management experience
Preferred Qualifications:
- Experience with GxP regulations and IMP requirements
- Any experience with N-SIDE forecasting systems, IRT systems preferred
- Risk management experience.
Soft Skills:
- Demonstrated leadership experience in engaging and ensuring collaboration across different functions.
- Excellent workload priorization within a dynamic, timeline-driven, culturally diverse organization.
- Advanced organizational, planning, and prioritization skills with effective problem-solving and decision-making abilities.
- Excellent communication (written and oral), negotiation, and influencing skills.
- Ability to build and maintain efficient professional relationships with partners and stakeholders.
- Experience operating in cross-cultural and…
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