Clinical Supply Chain Project Leader Employer Sanofi Location Cambridge, Massachusetts Start date Sep 12, 2026 View more categories View less categories Discipline Clinical , Clinical Research , Manufacturing & Production , Supply Chain Required Education Bachelors Degree Position Type Full time Hotbed Genetown Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details Job title :

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 Sanofis mission where deep immunoscience meets bold, AI-powered research. In R D, youll drive breakthroughs that could turn the impossible into possible for millions.

About Sanofi:

Were an R D-driven, AI-powered biopharma company committed to improving peoples 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 peoples lives.

Main responsibilities:

CSC Strategy & Implementation Define and implement clinical supply chain strategy aligned with CSC KPIs and project objectives Assess study design feasibility (ID study 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:

Bachelors 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 its 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 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. #GD-SA #LI-SA #vhd #LI-Hybrid 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. Company Pursue Progress. Discover Extraordinary. Science has been our calling from the beginning. Sanofi's heritage of turning the impossible into the possible stretches back to the 19th century — a rich history of healthcare innovation built by diverse companies united by one shared purpose. More than 150 years later, that spirit lives in everything we do and every person we serve — from the patients who take our medicines, to the healthcare professionals who trust us, to the 83,000+ employees and communities around the world who make it all possible. And today, we're writing the next chapter of that legacy. We are an R D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Better is out there. Better medications, better outcomes, better science. And it all starts with people like you — from different backgrounds, in different locations, doing different roles — united by a single mission: we chase the miracles of science to improve people's lives. Take the most important step in your career and help us change the lives of patients, families, and communities for the better. Company info Location Cambridge Massachusetts United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Sr Specialist Indirect Procurement Hyderabad, India Staff Supply Network & Capacity Planning Specialist, Advanced Therapies Troy, New York Director, Clinical Supply Chain Operations Bridgewater, NJ