A typical workweek for an RN at Eli Lilly involves coordinating and monitoring clinical trial activities, supporting participant safety and protocol adherence, and collaborating closely with clinical research associates, physicians, and regulatory teams. You may be responsible for data collection, patient assessments, adverse event reporting, and ensuring compliance with regulatory standards. Regular meetings and cross-functional collaborations are common, and you will often need to adapt to evolving study demands. The environment is generally fast-paced and dynamic, providing exposure to cutting-edge medical research and opportunities to develop expertise in clinical trials.