Associate / Sr. Associate - Clinical Trial Supply Management At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We're looking for people who are determined to make life better for patients around the world.
Main Purpose and Objectives of Position: The Clinical Drug Supply organization team is accountable for partnering with drug development teams, clinical, PRD, and the broader Product Delivery Organization to enable innovative supply chain solutions and speed the delivery of clinical trial materials for patients. This is accomplished by planning and scheduling via a Material Requirements Planning (MRP) system (SAP) and communications with key business partners.
The Clinical Trial Supply Management Associate is responsible for collaborating with the Product Delivery Supply Senior Director, Clinical Trial Supply Managers, Molecule Planners, and the broader Product Delivery organization to support supply chain planning and execution for all molecules and trials in development. This role involves developing demand forecasts and inventory management strategies at hubs, depots, and sites, and executing the strategy in partnership with supply planning staff and cross-functional operational teams.
Key Responsibilities: Make quality culture the foundation of your work, to ensure our products are safe and effective. Collaborate with Product Delivery Supply Senior Directors, Clinical Trial Supply Managers, and Molecule Planners to provide expertise in supply chain methodologies. Ensure adequate and timely supply of Clinical Trial (CT) Material to support CT execution. Utilize forecasting techniques and site inventory management tools to ensure CT Material supply at sites, hubs, and depots throughout the life of a trial. Create and deliver appropriate training and pharmacy manual creation related to CT material and supply. Maintain GMP/GCP compliance by following procedures applicable to CT execution. Communicate with affiliates, global team members, and external partners on timing for CT Material shipments and material availability. Problem solve CT Material issues in partnership with Supply Senior Director, Clinical Trial Managers, and Molecule Planners. Understand how supply strategy and demand forecasts impact Product Delivery and Business Unit/Research budgets. Support innovation and process optimization to speed drug development by influencing scenarios around supply strategies. Educational Requirements: • Bachelor's degree, preferably in health care or sciences related field or 3+ years work experience in supply chain management or clinical development.
Experience Requirements: Strong project management abilities (timeline, scope, budget, risk management). Demonstrated problem-solving skills for complex issues. Strong organizational and collaboration skills. Effective communicator. Strong computer skills (i.e. Word, Excel, PowerPoint, Microsoft Project). Language Requirements: Must speak and write fluent English.
Additional Information/Requirements: Domestic and international travel may be required (10%). Work outside of core hours may be required to support the portfolio across the globe.
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