Clinical Supply Chain Lead | AI-Driven Biopharma

Sanofi; Cambridge (MA); Hybride; USD 120 000 - 180 000; Plein temps

Avantages offerts par ce poste

Health benefits

14 weeks parental leave

Wellness programs

Career growth and international moves

Résumé du poste

Sanofi seeks a Clinical Supply Chain Project Leader to drive IMP supply, ensuring timelines, quality, and budget compliance for assigned projects. You will define CSC strategy at the project level and oversee study management activities, aligning with global standards and KPIs.

You will lead cross-functional teams, manage risks, and communicate with stakeholders to drive continuous improvement and successful trial execution in a dynamic, international environment.

Qualifications

• Education: Bachelor’s degree with 5+ years OR Master’s with 3+ years in Health Sciences or related fields.
• Experience in pharmaceutical industry, especially clinical supply chain, clinical operations, or manufacturing.
• Project Management experience.

Responsabilités

• Define and implement clinical supply chain strategy aligned with project objectives and CSC KPIs.
• Oversee study management activities ensuring adherence to plan and GCP/GMP standards.
• Manage risk, monitor plan execution, and implement mitigation plans.
• Coordinate with project team; lead CSC-Study Leaders and stakeholders.
• Report progress and issues to CSC Leadership Team and drive process improvements.

Connaissances

Project management

Pharmaceutical industry experience

Leadership

Communication

Time management

Cross-functional collaboration

Formation

Bachelor's or Master in Health Sciences or related

Outils

N-SIDE forecasting systems

IRT systems

Description du poste

Sanofi seeks a Clinical Supply Chain Project Leader to drive IMP supply, ensuring timelines, quality, and budget compliance for assigned projects. You will define CSC strategy at the project level and oversee study management activities, aligning with global standards and KPIs.

You will lead cross-functional teams, manage risks, and communicate with stakeholders to drive continuous improvement and successful trial execution in a dynamic, international environment.