Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases. The Role: Reporting to the Senior Director, Global Supply Chain and Logistics, this position is responsible for integrated clinical and commercial product planning. The Associate Director, Supply Chain Product Planning, partners with the clinical supply chain, commercial supply chain, CMC-project management, CMC-QA, and CMO project core teams to obtain forecasts, which the Associate Director will then use to generate/update the master production schedule across multiple, global, external CMOs. This role also monitors global stock levels, sets safety stock guidelines, tracks expirations, and allocates bulk materials. Key Responsibilities: Develop and maintain the combined clinical and commercial forecasts within the supply chain management system (SCMS) planning and inventory management tool based on actual demands and future projection inputs from clinical and commercial teams. Translate clinical trial enrollment schedules and commercial sales forecasts into the master production plan for drug substance, drug product, drug/device combination products, clinical finished goods, and commercial finished goods. Allocate drug substance batches to clinical versus commercial end use, considering Regulatory-driven material requirements. Build and maintain item/material masters within SCMS tool. Contribute supply chain input into cross-functional CD&OP/S&OP processes. Provide supply plan requests to CMO core teams at vendor-specific frequency and integrate endorsed manufacturing schedules into master production plan within the SCMS. Generate and communicate bulk material allocations and associated finished goods production plans to clinical and commercial supply colleagues to support operational execution of finished good batch production at packaging and labeling vendors. Establish safety stock guidelines for materials across the global supply chain, project future inventory positions, and prevent overstocking or stockouts for clinical and commercial materials. Monitor global stock levels, safety stock, and expiration dates. Respond to dynamic clinical and commercial projections by developing/comparing various scenarios and determine/communicate the associated impact across end-to-end materials. Partner with finance to determine the budget impact of various planning scenarios. Identify supply bottlenecks, manage lead times, and maintain operational continuity under strict GxP rules. Support commercial launch readiness activities. Requirements: Bachelor’s degree in…