Job title: Clinical Supply Chain Project Leader
About the Job
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:
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Defines and implements the CSC Strategy at project level.
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Oversees study management activities ensuring adherence to plan.
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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
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Define and implement clinical supply chain strategy aligned with CSC KPIs and project objectives
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Assess study design feasibility (ID study card, Abbreviated Protocol stages) and optimize project delivery
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Influence Label &Pack outsourcing and distribution network strategy decisions
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Monitor supply chain performance (cost, lead times, quality) using KPIs and digital tools
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Drive continuous improvement and innovation across clinical supply chain operations
Study Management Oversight
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Lead CSC-Study Leaders and oversee all operational activities ensuring compliance with GCP/GMP standards
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Ensure CSC strategy harmonization across multiple trials with adherence to timelines and budget
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Monitor plan execution, identify risks, and implement mitigation plans
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Identify opportunities to streamline processes and reduce lead times and costs
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Serve as primary point of contact for project team and coordinate PAI preparation
CSC Representation & Stakeholder Communication
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Provide CSC expertise and contribute to project decision-making in project meetings.
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Escalate IMP/device/AxMP/comparator issues and propose mitigation strategies
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Interact with GPH, CMC leaders, and Clinical leaders to integrate CSC requirements into project strategy
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Report Progress and issues to CSC Leadership Team
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Facilitate knowledge sharing and provide feedback on contractor performance
About You
Education:
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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:
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Experience in pharmaceutical industry, preferably within clinical supply chain, clinical operations, or manufacturing environments.
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Project Management experience
Preferred Qualifications:
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Experience with GxP regulations and IMP requirements
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Any experience with N-SIDE forecasting systems, IRT systems preferred
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Risk management experience.
Soft Skills:
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Demonstrated leadership experience in engaging and ensuring collaboration across different functions.
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Excellent workload prioritization within a dynamic, timeline-driven, culturally diverse organization.
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Advanced organizational, planning, and prioritization skills with effective problem-solving and decision-making abilities.
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Excellent communication (written and oral), negotiation, and influencing skills.
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Ability to build and maintain efficient professional relationships with partners and stakeholders.
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Experience operating in cross-cultural and complex organizational matrices.
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Self-driven with effective time management skills.
Why Choose Us
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Bring the miracles of science to life alongside a supportive, future-focused team.
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Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
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Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
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Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
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Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
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Help improve the lives of millions of people globally by making drug development quicker and more effective.
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Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.