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 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.
Purpose:
The Clinical Drug Supply (CDS) organization is responsible for strategically planning and supplying materials, trial support services and innovative capabilities to support the execution of clinical trials globally for all business units across all phases of development. This group is within the Clinical Capabilities organization and partners across functions within the Clinical Design, Delivery & Analytics (CDDA) and Product Research & Development (PRD) to influence trial design and provide solutions to operationalize these trials and enable asset strategies across the portfolio.
The role of the Clinical Trial Commercial Product, Buyer Planner (CPBP) is to ensure a robust strategy and integrated plan for supplying Commercial Products that supports Lilly Clinical Trials, externally sponsored research, Expanded Access Programs, and decentralized and clinical material trial regulations. The CPBP will use their global expertise for commercial products (procurement, wholesalers, supply chain, etc.) in developing strategies for supplying commercial products to support clinical trials. The CPBP is accountable for development of the Materials Master Requirements Plan, purchasing decisions, and management of Product Delivery (PD) material flow to meet required timelines. Moreover, the CPBP will use their supply chain expertise to influence demand forecasts and leverage innovative sourcing strategies.
This role is critical in delivering the Lilly portfolio and key development milestones. The CPBP will anticipate and resolve technical issues with the supply chain and drive for solutions that meet the needs of the business. The CPBP will collaborate with Supply Planning to ensure the commercial product strategy meets the demands of the molecule/study plan as well as partners with the Commercial Product Material Coordinator to ensure execution of the strategy.
Key Responsibilities:
1. Participate in demand planning and sourcing strategy decisions considering regulatory requirements at a study and asset level through partnership with Supply Planning, Quality and Clinical.
2. Have supply chain planning responsibility for Commercial Products, Lilly and Non Lilly, to meet the demand plan supporting Lillys clinical trials and externally sponsored research.
3. Work closely with Clinical Trial Supply Managers to understand trial operating model and any