Manager, Supply Chain Management

Responsible for the end-to-end material management of cGMP materials as well as managing the supply chain on single or multiple clinical studies working closely with Clinical Operations, Regulatory Affairs, Quality, Development, Manufacturing, Analytical Development and the Supply Chain Management team. This includes leading complex studies that will require global interactions, and ensuring changes in supply configuration, trial design, enrollment timelines, manufacturing availability, and regulatory requirements are considered. Additionally, will coordinate and lead supply activities with both internal and external partners and serve as a key point of contact with multiple functional areas. Maintain inventory oversight of applicable drug supply in collaboration with other functions in Development, Manufacturing & Supply. Support logistics execution and oversight of DS and DP supply Assist with assembly of bulk devices and allocation across studies as applicable. Develop and execute Demand & Operations Planning with Supply Chain Management team and other cross-functional members, such as Clinical Operations and Manufacturing. Position requires up to 20% travel (domestic and international) including 2 times per year for All Hands meetings.