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Eli Lilly and Company Clinical Trial Supply Management - R-4586 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 39,000 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.The Clinical Trial Supply Management Consultant is responsible for:The Clinical Supply Planning and Execution (CSPandE) function 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.Collaborating with the Product Delivery Supply Advisor and the broader Product Delivery organization to influence clinical trial design and supply chain strategy for all molecules and trials in development, including the most sophisticated.Developing demand forecasts and inventory management strategies at hubs, depots, and sites then executing the strategy with cross-functional operational teams.In this role, you will be the primary contact to the global clinical team for the trials they support.Driving 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:Be an active and engaged member of the global trial development team influencing trial designs and protocol language around all aspects of clinical supply.Translate protocol or planned protocol requirements into demand forecastInfluence 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 processesPerform 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 necessaryMaintain GMP/GCP compliance by following follow procedures applicable to clinical trial executionCreate, review, and/or approve appropriate documents outlined in business processesAppropriately raise issue identification through solutions within Product Delivery and to the clinical function as it relates to CT supply.Understand how supply strategy and demand forecast affects Product Delivery and Business Unit/Research budgets, communicate cost considerations for various trial supply options as an input into decision making, and proactively manage communication around changes that impact the Product Delivery budget for a trial.Provide information, as requested, for budget development and/or changes to an existing budget as they relate the demand forecast or supply strategy.Reach across boundaries and integrate information from external and internal collaborators to bring together diverse perspectives for supply plans.Support innovation and process optimization to speed drug development by influencing scenarios around supply strategies and business process improvement.Fostering an environment of integrated teamwork via shared learning, accountability, influencing others without authority.Basic Requirements: Bachelors degree, preferably in health care, business or sciences related field with 5 years work experience in supply chain management or clinical development.Additional Preferences: Demonstrated ability to understand the supply chain needs of various trial designsProven ability to effectively partner/influence cross functionally to delive

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