Global Clinical Supply Chain Leader

Sanofi Group; Cambridge (MA); Híbrido; USD 120.000 - 150.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health benefits

Parental leave

International opportunities

Career growth

Descripción de la vacante

Sanofi Group in Cambridge, MA seeks a Clinical Supply Chain Project Leader to own IMP supply timelines, quality and budget for a project. You will define CSC strategy at the project level, oversee study management activities, and represent CSC in cross-functional meetings.

You will drive continuous improvements, coordinate with GxP/GMP partners, mitigate risks, and ensure timely communication with stakeholders. Join a fast-paced, AI-powered biopharma environment shaping patient outcomes.

Formación

• Bachelor’s degree with 5+ years OR Master’s degree with 3+ years preferably in Health Sciences or related disciplines (Engineering, Pharmacy, Chemistry, Biology, etc.)
• Experience in pharmaceutical industry, preferably within clinical supply chain, clinical operations, or manufacturing environments.
• Project Management experience
• Experience with GxP regulations and IMP requirements

Responsabilidades

• Define and implement clinical supply chain strategy aligned with CSC KPIs and project objectives
• Oversee study management activities ensuring adherence to plan
• Coordinate PAI preparation and be primary CSC contact
• Monitor supply chain performance using KPIs and digital tools
• Drive continuous improvement and innovation across clinical supply chain operations

Conocimientos

Project Management

Leadership

Communication

Cross-functional work

GxP knowledge

Educación

Bachelor’s degree in Health Sciences or related disciplines

Master’s degree in Health Sciences or related disciplines

Herramientas

N-SIDE forecasting systems

IRT systems

Descripción del empleo

Sanofi Group in Cambridge, MA seeks a Clinical Supply Chain Project Leader to own IMP supply timelines, quality and budget for a project. You will define CSC strategy at the project level, oversee study management activities, and represent CSC in cross-functional meetings.

You will drive continuous improvements, coordinate with GxP/GMP partners, mitigate risks, and ensure timely communication with stakeholders. Join a fast-paced, AI-powered biopharma environment shaping patient outcomes.