Jobs at Eli Lilly and Company

Provides PK/PD and quantitative clinical pharmacology leadership across drug discovery and development. Leads exploratory MIDD analyses, study protocols, analysis plans, regulatory documents, and data-driven development decisions. Supports FDA, EMA, and PMDA interactions, communicates quantitative insights to cross-functional stakeholders, mentors scientists, and represents the organization through publications and industry leadership.

Provide high-level administrative and chief of staff support to the VP of Protomer. Responsibilities include project tracking, managing calendars, organizing meetings, coordinating travel, and overseeing site initiatives while ensuring effective communication and collaboration with internal and external stakeholders.

Provides technical leadership for peptide API manufacturing at external contract manufacturers. Responsibilities include process monitoring, validation, technical issue resolution, root cause analysis, CAPA development, regulatory compliance, process optimization, continuous improvement, and reliable commercial supply. The role also requires cross-functional collaboration, technical transfer support, process knowledge management, and coaching of colleagues. Occasional international travel and access to manufacturing and laboratory areas are required.

Oversee daily QA statistical sorting operations, including syringe defect kit management, scheduling, GMP document review, visual syringe inspection, deviation and change-control support, training, and inspection readiness. The role supports site start-up, commissioning, qualification, safety initiatives, process improvement, and development of QA assistants and parenteral visual inspectors. Overtime, off-shift support, physical mobility, and lifting up to 30 pounds may be required.

Owns hands-on engineering delivery for clinical supply and delivery platforms, including AWS and Databricks data platforms, APIs, microservices, integrations, cloud infrastructure, observability, and AI/agentic workflows. Designs databases, pipelines, and lakehouse solutions; implements GxP/GCP compliance and audit readiness; and prototypes production capabilities. Provides architecture guidance, code reviews, mentorship, technical decision-making, and cross-team leadership while remaining an active individual contributor.

Owns LillyDirect’s end-to-end consumer experience strategy, mapping journeys, identifying friction, synthesizing research and analytics, monitoring funnel health, and guiding product-pod prioritization. The role advocates for consumers, translates insights into roadmap opportunities, tracks competitive benchmarks, facilitates cross-functional workshops, and communicates strategy to executives. It requires collaboration with product, design, engineering, legal, compliance, regulatory, market research, and analytics teams.

Leads cross-functional clinical study teams through trial planning, execution, enrollment, risk mitigation, budgeting, vendor oversight, regulatory readiness, and closeout. Owns timelines, Trial Master File inspection readiness, communications, and regional operational coordination. Applies clinical, scientific, regulatory, and Good Clinical Practice expertise to support trial design, agency interactions, issue resolution, and continuous improvement. Periodic travel to investigator meetings and scientific or regional symposiums is required.

The Associate Director leads complex clinical trials, ensuring delivery of milestones while managing budgets, timelines, and risks across global teams. Key responsibilities include project management, cross-functional team leadership, and maintaining trial integrity and compliance with regulations.

Lead statistical programming for clinical trials including creation of SDTM and ADaM datasets, generation of tables/listings/figures, authoring Define/RG/CRT packages, collaborating on statistical analysis plans, selecting and implementing statistical methods, peer-reviewing outputs, and supporting regulatory submissions while maintaining SAS proficiency.

Lead ServiceNow platform delivery and operations for ITSM modules, ensuring platform stability, SLA performance, automation/agentic AI adoption, governance, and team development across India while partnering with global stakeholders.

Provides strategic and technical leadership for Lilly’s eDiscovery program across the full EDRM lifecycle. Manages legal hold systems, data preservation and collection, processing, review, production, vendor relationships, workflows, and chain-of-custody requirements. Evaluates AI, machine learning, TAR/CAL, predictive coding, and analytics solutions while ensuring defensible legal processes. Partners with Legal, Privacy, Records Management, IT, Compliance, Cybersecurity, outside counsel, and business stakeholders, and mentors team members.

Generate high-quality recombinant DNA and protein reagents supporting pharmaceutical drug discovery and clinical programs. Responsibilities include vector construction, protein expression, purification, refolding, antibody labeling, and protein standard generation. The role involves independently managing projects with limited supervision, collaborating across a multidisciplinary team, providing technical expertise, improving processes, and resolving reagent-generation challenges.

Leads private-market expansion for obesity treatments across Israel, developing go-to-market strategies, strategic partnerships, reimbursement and pricing models, and policy initiatives. Builds C-suite relationships with insurers, employers, pharmacy chains, telehealth providers, and private healthcare networks. Drives commercial adoption, revenue growth, supply-chain integration, stakeholder engagement, and data-driven value propositions while coordinating with market access, marketing, sales, and commercialization teams.

Builds and sustains AI-enabled information infrastructure, process visualizations, dashboards, and knowledge-management systems for pharmaceutical R&D and manufacturing value streams. Maps cross-functional processes, surfaces KPIs and constraints, supports daily management, coaches teams on operational excellence, and provides leadership-ready performance insights. Partners with scientific and operational subject matter experts to ensure accurate content, improve process maturity, reduce manual data work, and enable continuous improvement across the division.

Supports global employee expense operations using SAP Concur by reviewing policies, providing Tier 1 support, resolving system and interface issues, administering credit cards, assisting with post-payment audits, preparing metrics, testing enhancements, and supporting process-improvement projects. The intern manages inquiries, performs reporting and analysis, maintains compliance controls, and collaborates with affiliates and cross-functional teams.

Lead end-to-end ML architecture, feature engineering, and production pipelines. Design/deploy CI/CD (Docker, Kubernetes, GitHub Actions), monitor production ML/LLM systems, build agentic AI using LangGraph, implement RAG with vector DBs like Pinecone, establish LLMOps practices, define APIs/contracts with partner teams, and provide technical oversight to junior engineers.

Leads global regulatory strategy and execution for immunology medicines from candidate selection through end of lifecycle. Oversees FDA submissions and agency interactions, guides cross-functional regulatory teams, aligns regional plans, manages labeling and risk strategies, and supports global development and commercialization. Builds external stakeholder relationships, advises marketing and communications teams, mentors regulatory personnel, and represents regulatory affairs in governance forums.

Lead development of scalable digital health platform solutions, establishing software architecture and development standards while coordinating multiple technical teams. Evaluate designs, manage software delivery risks, support regulatory and medical device quality expectations, and drive platform innovation through proofs of concept. Mentor developers, influence architects and delivery teams, and guide Agile development across Lilly and external partners. The role requires expertise in cloud platforms, asynchronous systems, identity management, CI/CD, and software lifecycle delivery.

Lead architecture and technical direction for digital health software platforms while managing a team of 2–5 engineers. Responsibilities include approving system designs, guiding cloud and asynchronous integrations, managing performance and capacity, driving innovation roadmaps, supporting cybersecurity and regulatory compliance, establishing engineering standards, mentoring technical leaders, and coordinating delivery across product, design, operations, and business teams.

Develop and deploy analytical methods for small-molecule drug discovery across cheminformatics, computational biology, statistical modeling, and AI/ML. Translate scientific challenges into analyses supporting compound prioritization, design recommendations, and mechanism-of-action hypotheses. Collaborate across data, architecture, automation, and AI teams to create production-ready, agent-accessible capabilities. Evaluate emerging methods through benchmarking, address data gaps, publish research, present at conferences, and advise scientific teams.