Clinical Supply Chain Project Leader
Job in
Cambridge, Middlesex County, Massachusetts, 02138, USA
Listed on 2026-07-13
Listing for:
Sanofi
Full Time
position Listed on 2026-07-13
Job specializations:
-
Business
Regulatory Compliance Specialist, Operations Management
Job Description & How to Apply Below
Clinical Supply Chain Project Leader
* Location:
Cambridge, MA
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:
* 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
Study Management Oversight
* 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
CSC Representation & Stakeholder Communication
* 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
About You
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 prioritization 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 complex organizational matrices.
* Self-driven with effective time management skills.
Why Choose Us
* Bring the miracles of science to life alongside a supportive, future-focused team.
* Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
* Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
* 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.
* 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.
* Help improve the lives of millions of people globally by making drug development quicker and more effective.
* 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…
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