Senior Manager, Global Clinical Supply Chain Planning

Role: Senior Manager, Planning Lead responsible for developing end-to-end clinical supply chain strategies for innovative medicines in development. Objectives include translating clinical trial protocols into detailed supply plans, forecasting requirements, and managing supply-demand scenarios to mitigate risks. Responsibilities span coordinating with clinical operations, pharmaceutical sciences, logistics, and quality teams to ensure supply integrity, compliance, and timely delivery across global sites. Key tasks involve scenario planning, inventory management, risk assessment, and maintaining supply models, utilizing systems like ClinApps CSMD. Qualifications: Bachelor's degree in Engineering, Management, Pharmacy, or related field; 6+ years in pharmaceutical supply chain or related experience, preferably in GxP environments. Skills include stakeholder influence, project management (MS Project or similar), and GxP compliance knowledge (GMP, GDP, GCP). High-value specifics: focus on clinical development phases, including complex supply scenarios, regulatory compliance for global trial supply, and cross-functional stakeholder engagement. Location: Lexington, MA, full-time, hybrid work setup, with no travel specified.