Clinical Supply Chain Project Leader

BioSpace; Cambridge (MA); In loco; USD 140.000 - 170.000; Tempo pieno

Descrizione del lavoro

Sanofi is seeking a Clinical Supply Chain Project Leader in Cambridge, MA, to oversee IMP supply, timelines, quality and budget for multiple studies. You will define CSC strategy at the project level and lead study management with stakeholders, driving process improvements and global initiatives.

Strong leadership and communication across cross-functional teams are essential. Join Sanofi’s mission to accelerate drug development, leveraging AI-powered research and cutting-edge platforms to

Competenze

• Experience in pharmaceutical industry, preferably within clinical supply chain, clinical operations, or manufacturing environments.
• Project Management experience.
• Experience with GxP regulations and IMP requirements.
• Experience with forecasting systems (N-SIDE) and IRT systems preferred.

Mansioni

• CSC Strategy & Implementation: Define and implement clinical supply chain strategy aligned with CSC KPIs and project objectives.
• Study Management Oversight: Lead CSC-Study Leaders and oversee all operational activities ensuring compliance with GCP/GMP standards.
• CSC Representation & Stakeholder Communication: Provide CSC expertise and contribute to project decision-making in project meetings.
• Monitor supply chain performance using KPIs and digital tools; drive continuous improvement across operations.
• Identify risks, mitigate issues, and coordinate PAI preparation with project teams.
• Collaborate with GPH, CMC and Clinical leaders to integrate CSC requirements into project strategy.

Conoscenze

Project Management

Leadership

Communication

Cross-functional Collaboration

GxP Knowledge

IMP/CMC Knowledge

Formazione

Bachelor's degree in Health Sciences or related discipline

Master's degree in Health Sciences or related discipline

Descrizione del lavoro

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.

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

We're 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

Education

About You

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 Affimative 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.