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Eli Lilly and Company Clinical Trial Supply Management Consultant - R-13235 in Indianapolis, Indiana

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 35,000 employees around the world 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 give our best effort to our work, and we put people first. Were looking for people who are determined to make life better for people around the world.Job DescriptionMain Purpose and Objectives of Position:The Clinical Supply Planning and Execution (CSPandE) function is accountable for partnering with drug development teams, clinical, 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 system and communications with key business partners.The Clinical Trial Supply Management Consultant (CTSM)is responsible for collaborating with the Product Delivery Supply Advisor and the broader Product Delivery organization to influence clinical trial design and supply chain strategy. The CTSM Consultant develops demand forecasts and inventory management strategies at hubs, depots, and sites. This drives planning and execution activities across Product Delivery, internal and external manufacturing, packaging, and distribution plants around the globe. They execute the strategy along with cross-functional operational teams. The CTSM Consultant is the primary contact to the global clinical team for the trials they support. The CTSM Consultant will drive robust, strategic discussions with their clinical and functional counterparts to develop different supply scenarios that meet trial intent while looking for efficiencies and speed.Key Responsibilities:Collaborate with Product Delivery Supply Advisors and Molecule Planners to provide expertise in supply chain methodologies while continually looking for internal and external advancements to grow technical expertise and drive processes improvements for productivity and efficiency gains.Be an active and engaged member of the global trial development team influencing trial designs and protocol language around all aspects of clinical supply.Ensure adequate and on time supply of Clinical Trial (CT) Material to support CT execution.Translate protocol or planned protocol requirements into demand forecast:Influence supply strategyDetermine appropriate operating model for forecasting and calculate the forecast with appropriate business-approved tool and processes.Manage accurate CT Material demand forecast via MRP System (SAP) per business processesRegularly re-evaluate the demand forecast to align with CDandOPCreate and deliver appropriate training and pharmacy manual creation as it related to CT material and supplyUtilize forecasting techniques and site inventory management tools to ensure CT Material supply at sites, hubs, and depots throughout the life of a trialCoordinate initial shipment strategy and execution to clinical sitesUse systems and tools to maintain proper inventory levels and on time, shipment forecastsPerform trial-level risk assessments on CT Material quantities and expiry dates throughout life of trialCalculate and re-assesses quantities for trial-level import permits, as necessaryEnsure proper destruction of material, as appropriateMaintain GMP/GCP compliance by following follow procedures applicable to clinical trial executionCommunicate with affiliates, global team members, and eternal partners on timing for CT Material shipments and material availability.Problem solve CT Material issues including temperature excursions, material needs, shipment receipt and other issues.Create, review, and/or approve appropriate documents outlined in business processesCT Supply issue identification and resolution withi

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