Senior Manager, Clinical Supply Chain Management

Role: Associate Director, Clinical Supply Chain Management, responsible for strategic and operational leadership of global clinical supply for multiple studies across phases. Objectives: ensure continuous trial material availability, mitigate risks, and align cross-functionally with Clinical Operations, Quality, Regulatory, and external partners. Responsibilities: oversee supply planning, vendor management, packaging, labeling, comparator sourcing, distribution, and study closeout; develop demand forecasts, manage budgets, and ensure compliance with regulatory standards. Requirements: BS/BA with 6+ years in clinical supply chain within biopharma, experience managing multi-study programs, and vendor oversight including packaging/labeling organizations. High-Value: experience supporting early to late-stage clinical development, global distribution expertise, knowledge of cGMP, GCP, GDP, and regulatory requirements across US, EU, and APAC; strong project management and cross-functional influence skills. WorkSetup: based onsite in Lexington, MA; no travel specified.