Associate Director, Clinical Supplies-Global Planning & Operations

Associate Director, Clinical Supplies‑Global Planning & Operations Summit Therapeutics Inc. is a biopharmaceutical oncology company dedicated to improving quality of life, extending patient longevity, and addressing unmet medical needs. Summit values integrity, excellence, collaboration, and a commitment to its people. Overview of Role The Associate Director of Clinical Supply leads global clinical supply activities, ensuring timely and compliant delivery of clinical trial material (CTM) and investigational medicinal products (IMP). This role oversees demand and supply planning, inventory visibility, release and logistics readiness, vendor oversight, analytics, and continuous improvement, while partnering with cross‑functional stakeholders to develop and communicate supply strategies, timelines, budgets, and performance insights. Role and Responsibilities Clinical Supply Planning & Demand Under the direction of the Director, manage clinical supply manufacturing, distribution, and storage activities supporting global clinical trials and other R&D needs; coordinate, procure, and manage CTM/IMP supply for the Ivonescimab program. Establish and maintain a regular review cadence for supply plans against demand forecasts and confirmed orders; lead recurring demand and supply reconciliation meetings, identify short‑term constraints, and present mitigation plans. Manage bulk and packaged inventory and track/reconcile inventory across manufacturing, packaging, depots, and clinical sites. Coordinate upstream transport operations between suppliers and distribution warehouse(s) to support CTM/IMP supply. Maintain supply forecasts (creation, updates, cancellations) and communications in alignment with supplier agreements; review KPIs with suppliers and schedule regular governance/steering meetings; maintain inspection readiness through robust documentation workflows and archival of CTM/IMP supply documentation for the Trial Master File (TMF). Stakeholder Management & Partnership Liaise with Summit Program Management to build supply and demand plans for all pipeline activities; own, disseminate and amend as required. Partner with internal stakeholders and external suppliers to develop and communicate manufacturing and distribution plans, ensuring clinical supply objectives are supported. Interface with Quality Assurance (QA) and Qualified Person (QP) functions to plan release activities and facilitate timely disposition and release of CTM/IMP for further processing and shipment. Work closely with the Distribution/Logistics function to plan, document, and execute global cross‑border supply strategies, including controlled substances and global trade compliance requirements. Coordinate with Program Management and Regulatory teams; serve as owner of bulk CTM/IMP supply plans and timelines to ensure all product‑availability prerequisites are met. Operational Excellence and Continuous Improvement Ensure end‑to‑end inventory visibility, including management of material movements, utilization, expiry, returns, reconciliation, and destruction processes, leveraging appropriate systems and controls. Manage and oversee strategic and operational Clinical Supply Operations activities, driving standardization, analytics, and continuous improvement. Provide visibility of priorities to optimize QA/QP and regulatory release activities and support logistics and manufacturing operations, including coordination of expedited shipments when required. Evaluate and propose system improvements and technology enhancements; roll out and strengthen key IT systems to support supply planning and partner with IT to automate demand and supply data flows across systems. Define needs for data analytics capabilities to enable data‑driven insights across Clinical Supply; develop reporting and metrics (weekly/monthly as needed) to drive continuous improvement against key performance measures internally and with vendors. Create and manage reporting metrics and provide visibility to operations performance through report creation, insights, and analysis of system dashboards. Leadership Support annual budget planning through detailed cost‑of‑goods analysis and supplier‑level cost updates. Coach and mentor/line‑manage more junior staff; lead workstreams supporting departmental initiatives and goals; manage specialised or high‑profile projects; and serve as backup to the Director as needed. All other duties as assigned Experience, Education, and Specialized Knowledge and Skills Degree in Pharmacy, Engineering, or other scientific/technical field, or significant job‑related experience. Minimum 8+ years of relevant pharmaceutical industry and/or contract/service provider experience (preferred). Minimum 5+ years of relevant supply chain planning experience. Background in biological product manufacture is preferred. Strong understanding of cGMP requirements and regional regulatory drivers. Proficiency in software applicable to demand planning/forecasting and proficiency with Excel and MS Project (or equivalent project management software) is a plus. Line management experience is preferred. Pay Transparency

$175,000 - $200,000 USD

Actual compensation packages are based on factors unique to each candidate, including but not limited to skill set, depth of experience, certifications, and work location. Compensation may vary by location and can include bonus, stock, benefits, and other variable elements. Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining a diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. #J-18808-Ljbffr Summit-Therapeutics