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Clinical Supply Chain Project Leader

Sanofi EU -
Cambridge, MA

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Job Details

$105,000.00 - $151,666.66 a year
8 days ago

Benefits

Parental leave

Qualifications

Managing projects

Full Job Description

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 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 (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:

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 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.

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