Jobs at Eli Lilly and Company

Lead biochemistry strategy and assay development for oral macrocyclic peptide discovery, from lead identification through optimization and early clinical support. Develop and execute protein-binding and biochemical assays, characterize protein reagents, troubleshoot screening workflows, and enhance laboratory automation. Collaborate with biology, protein expression, ADME, safety, and PK/PD teams while providing scientific rationale, experimental planning, data interpretation, and project leadership.

Leads clinical development programs for diagnostic radiopharmaceutical imaging across oncology, immunology, and cardiovascular disease. Defines study strategies, endpoints, imaging criteria, biomarkers, and patient populations; interprets molecular imaging data and performance metrics; guides image-analysis validation; and collaborates with physicians, scientists, CROs, academics, software developers, and scanner manufacturers. Authors clinical and regulatory documents, evaluates emerging imaging technologies and AI, and communicates findings through presentations and publications.

Provides statistical leadership for pharmaceutical clinical development programs, including trial design, protocol and statistical analysis plan development, data analysis, regulatory submissions, scientific communications, and interpretation of results. Leads innovative statistical methodology, collaborates across data sciences and therapeutic-area teams, responds to regulators, peer-reviews statistical work, and influences clinical and business decisions.

Leads Lilly’s enterprise pandemic preparedness, infectious disease risk management, and public health emergency response strategy. Establishes governance, readiness metrics, response plans, continuity strategies, and crisis leadership structures across research, clinical development, manufacturing, supply chain, and corporate functions. Monitors infectious disease intelligence, advises executives and the Board, coordinates cross-functional emergency responses, develops public health partnerships, and oversees preparedness training, simulations, and after-action programs.

Manages the full lifecycle of procurement-facing contracts supporting oncology discovery and development. Responsibilities include drafting, negotiating, tracking, and ensuring compliance for scientific engagements; advising business partners; coordinating with Legal, Project Management, Procurement, and research teams; managing suppliers and contract risks; supporting procure-to-pay activities; and maintaining accurate records in the contract lifecycle management system.

Leads clinical data management for global development programs, including data strategy, electronic trial system implementation, data standards, validation, quality oversight, vendor management, reporting, documentation, and regulatory compliance. Partners with CROs and cross-functional teams to deliver accurate, timely clinical data and support submissions, inspection readiness, and clinical milestones across complex Phase I–III studies.

Leads LillyDirect’s forward-looking Consumer and HCP marketing strategy, growth investments, content briefing, innovation pipeline, competitive intelligence, and partnership alignment. Sets goals, KPIs, budgets, and testing strategies; advises senior leadership on investment priorities and scales successful marketing initiatives. Manages and develops marketing talent while fostering an inclusive, high-performing culture.

Leads clinical development programs for diagnostic radiopharmaceutical imaging across oncology, immunology, and cardiovascular disease. Defines study strategies, endpoints, imaging criteria, biomarkers, and patient populations; analyzes PET, SPECT, CT, and MRI data; evaluates imaging performance and advanced image analysis methods; and guides regulatory documentation. Collaborates with physicians, scientists, physicists, CROs, academics, software developers, and scanner manufacturers while communicating findings through publications and presentations.

Provide strategic patent counseling for key pharmaceutical assets: develop global patent filing and prosecution strategies, assess freedom-to-operate and IP risk, advise senior management, lead projects and task-directed teams, and drive continuous improvement in patent practice.