Eli Lilly currently has 36 active AI-related job listings. The majority of these roles, 56%, are focused on agents, with data-related positions making up another 28%. Engineering is the most frequent function for these hires. The company is primarily hiring in the United States and India. Frequent technology tags include agent orchestration, RAG, and model serving, indicating a focus on building and deploying AI systems.
Currently tracking 28 active AI roles, down 25% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $58k–$345k (avg $175k).
Eli Lilly currently has 36 active AI-related roles in our index. The most common open titles are: Director, Discovery Bioinformatics Oncology (2), Advisor - Agent Research, Advisor - Antibody Developability Validation & Benchmarking, Advisor - Data Architect, Data Foundry, Advisor - Lab Automation Software Engineer. Most positions are in Engineering and Research.
Eli Lilly's active AI hiring is concentrated in: agents (53%), data (25%), application (8%). These categories follow a seven-stage AI lifecycle: data, pre-training, post-training, serving infrastructure, agents, evaluation, and application.
Eli Lilly is hiring AI talent in: United States (29 roles), India (7 roles).
Job postings at Eli Lilly most frequently reference: agent orchestration, rag, model serving, llm observability, vector db.
In the past 30 days, Eli Lilly has posted 12 new AI-related roles. That is a -48% change versus the prior 30 days (23 → 12).
| Title | Stage | AI score |
|---|---|---|
| Director – Software Product Management, Enterprise AI Orchestration The Director of Software Product Management for Enterprise AI Orchestration at Eli Lilly will define and drive the strategy for deploying, managing, and optimizing AI agents and workflows at an enterprise scale within the pharmaceutical industry. This role involves owning the product roadmap for an enterprise AI orchestration platform, enabling business units to build and manage AI workforces, and ensuring AI investments deliver measurable business value while adhering to compliance requirements. | Agent | 7 |
| Director, Software Product Management – Discovery Research Platforms Product Management leader to shape strategy and development of custom software platforms for discovery research, focusing on computational drug design and optimization for large molecules. The role involves integrating agentic AI capabilities into research workflows, accelerating design-make-test-learn cycles, and enabling scientists to compose complex computational pipelines through AI-assisted interfaces. Requires partnership with computational biologists, protein engineers, and engineering teams to translate research needs into scalable software platforms. |
| Agent |
| 7 |
| Product Manager - GenAI Product Manager for GenAI products at Eli Lilly, focusing on defining vision, strategy, and execution. Requires experience with GenAI concepts, agent evaluation, and AI tools, bridging user needs with technical delivery in a healthcare context. | Agent | 7 |
| Director/Senior Director/ Executive Director: Digital Innovation & Technology Strategy – Global PK/PD & Pharmacometrics This role focuses on developing and implementing a digital strategy for integrating AI, ML, and automation into quantitative pharmacology and pharmacometrics workflows within a healthcare setting. The goal is to accelerate drug development, position the organization as an industry leader in AI-enabled drug development, and ensure scientific rigor and regulatory compliance. The role involves evaluating emerging AI technologies, leading pilots, partnering with IT and data science teams, driving AI adoption through organizational change, and defining success metrics. | Ship | 7 |
| Associate Director - Pricing Associate Director of Pricing at Eli Lilly Canada, responsible for developing and optimizing pricing and access strategies for the company's pharmaceutical portfolio. This role involves analyzing market data, informing reimbursement decisions, coordinating contracting, and managing regulatory compliance with PMPRB. The position requires significant pharmaceutical industry experience, strong analytical and communication skills, and the ability to influence without authority. While not directly building AI, the role leverages AI tools to automate work and requires understanding of AI's impact on business strategy. | — | 5 |
| Consumer Product Quality Assurance – Reporting & Insights Lead This role leads the transformation of reporting and analytics for consumer product quality assurance, converting complaint and quality data into validated, decision-ready insights. It involves defining and delivering a global strategy, partnering with IT for scalable solutions, and leveraging automation, AI, and advanced analytics to drive quality, compliance, and process improvements within a GxP-regulated environment. | — | 5 |
| Associate Director - LVA Strategy and Innovation This role focuses on accelerating innovation execution within Lilly Value & Access (LVA) by improving consumer experience, business model innovation, and the data/technology foundation. It involves seeking external solutions and internal process improvements through AI and other technologies, piloting initiatives, and collaborating with various stakeholders. The goal is to grow direct business, accelerate learning, enable data-driven decisions, and embed a consumer-centric mindset. | — | 5 |
| Associate Director - Ecosystem Growth & Contributor Partnerships This role focuses on growing and managing partnerships for an AI/ML platform (Lilly TuneLab) that provides drug discovery models to early-stage biotech companies. The Associate Director will be responsible for user activation, contributor onboarding, and developing strategic partnerships within the biotech ecosystem, acting as a liaison between the platform and external entities. The role requires a strong understanding of drug discovery and experience in business development or scientific partnerships. | — | 5 |
| Sr. Manager in Tech@Lilly The Sr. Manager in Tech@Lilly Business Capabilities and Operations team serves as the technology business partner to the CMO teams. This role is accountable for shaping and executing the HCP engagement technology strategy to enable broader reach, elevating the digital experience for HCPs, and driving scalable and high impact tech solutions. The role combines business partnership, tech leadership, solution integration, and innovation driver to empower and elevate HCP education impact. | — | 5 |
| ＜研究開発・メディカルアフェアーズ統括本部＞/Japan Data Sciences - Data Strategist Lead/Scientist/ Senior Scientist / Principal Scientist/ Sr. Principal Scientist/神戸本社・東京支社 This role focuses on developing and executing comprehensive strategies for acquiring, building, and utilizing real-world data (RWD) throughout the pharmaceutical lifecycle to enhance evidence generation. It involves leading RWD acquisition and development strategies, maximizing RWD utilization, ensuring quality assurance and dataset creation for analysis, and innovating data platforms with IT solutions. The role requires a Master's degree in Data Science, Medical Informatics, or Health Informatics, with at least 3 years of experience in data management and statistical analysis using RWD in clinical trials or observational studies. Strong communication skills in Japanese and English, and logical, scientific, and strategic thinking are essential. | — | 2 |
| Manager Global Supply Chain, IBU Manager Global Supply Chain responsible for analyzing demand and inventory data at IBU affiliates to ensure an accurate demand signal for the Global Sales and Operation Planning (GS&OP) process. This includes ensuring completeness of the demand statement in SAP, analyzing demand and production plan data, supporting new launches and post-approval changes, and potentially leading projects or supply chain processes for late-life cycle products. The role requires close collaboration with manufacturing sites and affiliate forecast coordinators to ensure medicines are available to patients. | — | 0 |
| Communication & Public Relations (PR) Intern (12-month) This is an internship role for a Communications & Public Relations student at Eli Lilly, a global healthcare leader. The intern will support various internal and external communication activities, including content creation, social media management, media relations, internal communications, and project management. The role requires strong writing, social media literacy, and basic design tool skills, along with detail-orientation and research abilities. The position is for a student pursuing a degree in Communications, Public Relations, Journalism, Marketing, English, or a related field, who must be returning to full-time studies after the internship. | — | 0 |
| Oncology Health-Outcomes Liaison The Health Outcomes Liaison (HOL) serves as the medical and HEOR interface between Lilly and U.S. population-based decision makers (PBDMs) including payers, health systems, research institutions, and policy makers. The HOL role provides answers to customer questions with clinical evidence, HEOR, and RWE to support formulary access and pathways/guidelines decisions impacting millions of patients. The HOL is acutely attuned to therapeutic evidence gaps, understands environmental trends, and anticipates stakeholder evidence needs. The HOL also works cross-functionally to provide external insights to influence strategy- especially the HEOR research agenda. | — | 0 |
| Senior Director - International Public Policy, (GCC, KSA, Türkiye & India) Senior Director of International Public Policy for Eli Lilly, focusing on the GCC, KSA, Türkiye, and India regions. This role involves developing and executing public policy strategies to support patient access, innovation, and business growth, while engaging with stakeholders and providing strategic counsel to leadership. Requires extensive experience in public policy within the life sciences industry and strong leadership in a matrixed environment. | — | 0 |
| Lilly StarT Marketing Intern - CMH, Türkiye Internship role in marketing for a pharmaceutical company, focusing on supporting brand managers, organizing events, and managing marketing materials. Requires proficiency in MS Office and AI tools. | — | 0 |
| ＜製造本部＞サプライチェーン ロジスティックス/P1-3/西神 Logistics Manager role within the manufacturing division of Eli Lilly, focusing on the strategic design, coordination, and management of logistics for raw materials, intermediate products, and finished goods. Responsibilities include optimizing transportation routes, managing warehouse operations, ensuring safety and quality compliance (GMP, GDP), managing external vendors, and contributing to global logistics initiatives. Requires strong analytical, communication, leadership, and project management skills, along with knowledge of logistics, production systems, and foreign language proficiency. | — | 0 |
| Site Compliance Leader The Site Compliance Leader at Eli Lilly is responsible for managing compliance to all regulatory requirements for next-generation biotech facilities. This role involves overseeing quality systems and processes, providing quality and technical expertise, and ensuring adherence to corporate quality standards and initiatives. The position requires extensive experience in quality assurance within the biotechnology or pharmaceutical manufacturing environment and a strong understanding of regulatory compliance. | — | 0 |
| Regulatory Affairs Sr. Associate/Manager Denmark & Iceland, This role is for a Regulatory Affairs Sr. Associate/Manager in Denmark and Iceland, responsible for affiliate regulatory lifecycle activities including marketing authorization, product launch, variations, and de-registration. The position involves interacting with local regulatory agencies, ensuring product information compliance, managing packaging materials, leading risk minimization plans, and maintaining regulatory documentation. It requires a Master's degree in a relevant field, proven experience in Nordic affiliate regulatory affairs, and fluency in Danish and English. | — | 0 |
| Health Technology Assessment (HTA) & PRA Lead, KSA This role focuses on Health Technology Assessment (HTA) and Pricing, Reimbursement & Access (PRA) within the Saudi Arabian healthcare market. The Lead will develop economic models, evidence packages, and HTA content for payer submissions, and design/deliver training programs for PRA and Key Account Management (KAM) teams to improve their economic fluency and payer engagement. The goal is to accelerate access for Lilly's innovations and sustain access for existing products in a maturing reimbursement environment. | — | 0 |
| Associate Director/Director – Risk Management Scientist Global Patient Safety Associate Director/Director role focused on risk management and patient safety within the pharmaceutical industry, requiring strategic guidance, development, and maintenance of risk minimization strategies, and collaboration with cross-functional teams and regulatory bodies. | — | 0 |
| Sr. Director, MSL Leader, CMH Mid Atlantic This role is for a Sr. Director, MSL Leader in the CMH Mid Atlantic region at Eli Lilly. The primary responsibility is to lead and manage a team of Medical Science Liaisons (MSLs), providing national field strategic leadership and ensuring effective interactions with Scientific and Clinical Experts. The role involves people leadership, field coaching, TA expertise, strategy integration, and operational excellence, ensuring compliance with all applicable policies and regulations. | — | 0 |
| Sr. Director, MSL Leader, CMH West This role is for a Sr. Director, MSL Leader in the CMH West region for Eli Lilly, a global healthcare company. The position focuses on leading and managing a team of Medical Science Liaisons (MSLs), providing strategic field leadership, and ensuring effective interactions with Scientific and Clinical Experts. Responsibilities include people leadership, development, field coaching, TA expertise integration, and operational excellence, ensuring compliance with regulations. | — | 0 |
| Manager - Discovery Operations, Early-Stage Oncology Manager in Discovery Operations (Operational Project Manager) experienced in external contract enablement, licensed biological material procurement/transfer, vendor relationship management, and domestic and international supply chain coordination, with some knowledge of third-party qualification processes. The role supports Oncology discovery portfolio by managing contractual and procurement enablement, prioritizing requests, and identifying operational risks. | — | 0 |
| Sr. Director - Quality, Concord Senior Director of Quality responsible for overseeing the Quality Management System, ensuring compliance with cGMPs, policies, and standards for parenteral manufacturing, device assembly, and packaging. The role involves strategic direction, quality objectives, continuous improvement projects, and leading/responding to regulatory inspections. | — | 0 |
| Manager - HO & PRA Manager for Health Outcomes & Pricing, Reimbursement, and Market Access (PRA) in Finland, focusing on Oncology & Hematology. The role involves developing and executing access strategies, leading reimbursement submissions and negotiations with Finnish authorities, and engaging with stakeholders to ensure timely patient access to Lilly's innovative treatments. This is an individual contributor role requiring deep knowledge of the Finnish healthcare system and strong negotiation skills. | — | 0 |
| Hospital Channel Manager Eli Lilly is seeking a Hospital Channel Manager in Warsaw, Poland, to oversee and develop the hospital distribution channel. This role involves coordinating with external partners, supporting commercial teams, monitoring wholesale and NFZ data, and contributing to channel strategy and B2B partnership models. The ideal candidate will have strong analytical skills, knowledge of pharmaceutical distribution, and business-level English. | — | 0 |
| Student Assistant - Patient Safety & Regulatory Affairs Student Assistant role supporting Patient Safety & Regulatory Affairs in the pharmaceutical industry, focusing on adverse event case management, literature monitoring, and translation of product information for Nordic countries. | — | 0 |
| Associate Director - Content Quality Review - Global Content Hub Associate Director for Content Quality Review within the Global Content Hub at Eli Lilly, responsible for managing scientific data and information delivery to various stakeholders, including regulators and healthcare professionals. The role involves managing a book of work, leading cross-functional teams, providing technical coaching on scientific content dissemination, and ensuring compliance with internal and external guidance. Key activities include portfolio management, people management and development, and document preparation for various medical affairs deliverables. | — | 0 |
| Medical Project Owner This role is a Medical Project Owner responsible for coordinating and tracking the end-to-end execution of medical and scientific content projects within Eli Lilly’s Global Content Hub. It focuses on project execution, workflow coordination, and operational visibility, ensuring projects move efficiently through initiation, development, review, approval, and closure. The role involves tracking milestones, managing workflows across tools like Veeva and Adobe Workfront, facilitating handoffs, and ensuring project setup and reporting accuracy. It is not an AI/ML development role. | — | 0 |
| Regulatory Manager, Ankara The Regulatory Manager in Ankara is responsible for supporting the local regulatory strategy and plan for assigned products, ensuring alignment with global strategies and local regulations. This role involves providing regulatory expertise for submissions, approvals, and local labeling, fostering operational excellence, and influencing local regulatory authorities. Key responsibilities include executing regulatory plans, ensuring compliance with local and global quality systems, managing labeling requirements, and identifying process improvement opportunities within the pharmaceutical industry. | — | 0 |
| Associate Director - eCOA Delivery Associate Director for eCOA Delivery at Eli Lilly, responsible for end-to-end planning, coordination, and delivery of electronic Clinical Outcome Assessment (eCOA) activities for clinical trials. This role involves managing project plans, cross-functional hand-offs, vendor deliverables, and risk mitigation to ensure timely and quality execution of eCOA builds and go-lives on the eCOA platform, adhering to GCP and 21 CFR Part 11 regulations. | — | 0 |
| Supply Chain Operations/OSSCE/Project Management Eli Lilly is seeking a Supply Chain Operations Specialist to manage projects, drive continuous improvement using Lean/Six Sigma, act as a SAP WM Classic SME, coordinate OSSCE, and steward Power BI analytics for warehouse and supply chain functions. | — | 0 |
| Associate/Sr. Associate/Manager - Lilly Ventures Tech Investing Associate to support and execute Lilly Ventures Tech Investing strategy, focusing on direct equity investments, fund-of-funds investments, and value pull-through. Responsibilities include data analytics, opportunity triage, reporting, and process optimization within the biotech and health tech innovation space. | — | 0 |
| Estágio - Relacionamento com o Cliente This is a customer relations internship at Eli Lilly, a healthcare company. The intern will provide information, register complaints, update customer data, collect adverse events, conduct patient education sessions, and manage patient support programs. The role requires a healthcare major, basic Microsoft Office knowledge, and desirable English skills. | — | 0 |
| Medical Advisor, Dermatology The Medical Advisor, Dermatology will serve as a core scientific expert on the Canadian Medical Affairs team, playing an integral role across launch activities, customer engagement, and evidence generation in dermatology. This role bridges medical strategy and local execution, working closely with cross-functional teams to ensure patients, healthcare providers (HCPs), and payers receive accurate, timely, and high-quality scientific information. Responsibilities include developing and executing medical strategy, managing budgets, providing medical education, engaging with stakeholders, supporting market access, collaborating on clinical research, and ensuring regulatory compliance. | — | 0 |
| Sr. Director - eCOA Program Lead This role is a Sr. Director level Program Lead for eCOA (electronic Clinical Outcome Assessments) within a specific therapeutic area at Eli Lilly. The role involves leading the strategy, delivery, governance, and continuous improvement of eCOA capabilities, serving as a senior point of contact between eCOA teams and clinical development stakeholders. Responsibilities include advising leadership, anticipating needs, resolving complex issues, managing escalations, contributing to platform strategy and roadmap, ensuring inspection readiness, and driving capability development. The role requires a strong background in clinical data management or drug development within the pharmaceutical/biotech/CRO industry, with preferred qualifications including experience with modern data technologies like AI/ML, RPA, and cloud systems, as well as familiarity with regulatory requirements like GCP and 21 CFR Part 11. | — | 0 |
| Sr. Regulatory Affairs Manager Senior Regulatory Affairs Manager at Eli Lilly in China, responsible for developing and implementing China registration strategies for pharmaceutical products, ensuring compliance with local and global regulations, and collaborating with cross-functional teams. The role involves overseeing the registration process, communicating with regulatory authorities, and potentially managing a team. | — | 0 |
| Sr. Manager Public Relations & Communications The Sr. Manager Public Relations & Communications at Eli Lilly plays a critical role in shaping and protecting the company's reputation within the Canadian healthcare sector. This role involves developing and executing integrated communications strategies, managing media relations, engaging with external stakeholders, and ensuring all communications align with business objectives and regulatory requirements. The position requires strong experience in the Canadian pharmaceutical or healthcare industry, excellent writing, project management, and media relations skills. | — | 0 |
| Senior Director, Commercial Insights & BD Forecasting This role is for a Senior Director of Business Development Forecasting & Analytics in the healthcare industry. The primary focus is on leading end-to-end commercial assessments for licensing, acquisition, and partnership opportunities, and building forecasting infrastructure. This involves developing expertise in new therapeutic areas, leading primary market research, and building flexible forecasting models. The role requires strong financial modeling skills and the ability to influence senior executives. | — | 0 |
| Associate Director, Clinical Research Lead (East Coast/Midwest) Associate Director, Clinical Research Lead responsible for driving clinical trial execution through investigator engagement and site performance management. This role requires deep therapeutic and scientific knowledge to influence investigators, elevate protocol understanding, and co-develop enrollment strategies. The CRL acts as a trusted partner to investigators and collaborates with internal teams to ensure quality, speed, and insight in trial delivery. Responsibilities include investigator management, clinical trial management, business development, and engagement with regulatory bodies. | — | 0 |
| (Sr.) Medical Science Liaison The Medical Science Liaison (MSL) role at Eli Lilly is focused on scientific and clinical expertise within specific therapeutic areas. MSLs serve as a key interface between Lilly Medical and external scientific and clinical experts (SEs/CEs), providing in-depth scientific and clinical information, gathering insights, and supporting research and clinical development. The role requires advanced scientific acumen, strong interpersonal and presentation skills, and strategic thinking to facilitate scientific exchange and address clinical care gaps for improved patient outcomes. | — | 0 |
| Administration Student - Finland This is an administrative student role in the pharmaceutical industry, focusing on supporting daily operations, project management, and vendor relations within a global healthcare company. The role requires strong organizational skills, proficiency in Microsoft 365, and the ability to work independently in a regulated environment. | — | 0 |
| Medical Science Liaison - Diabetes - Ottawa / ON East The Medical Science Liaison (MSL) will serve as a scientific resource for Canadian healthcare providers in the field of Cardiometabolic health, including Diabetes, Obesity and related disorders. The MSL's objective is to provide healthcare providers (HCPs) with the required scientific and clinical knowledge that meaningfully and precisely addresses their inbound requests. This role requires efficient and precise synthesis of the latest research on products, disease states, and standard of care within cardiometabolic health. | — | 0 |
| IDAP Batch Disposition This role is a Quality Assurance Representative responsible for the final disposition of semi-finished and/or finished drug combination products and packaging products. The primary focus is ensuring adherence to Global and Local Quality requirements and GMP standards for products released to the market. It involves batch disposition, leading/mentoring personnel on quality matters, providing guidance on quality systems, participating in inspections, and reviewing/approving GMP documents. The role also participates in process improvement initiatives. | — | 0 |
| Electronic Quality Systems Health & Performance Management This role focuses on establishing and leading the enterprise capability for continuous monitoring, trending, and risk-based oversight of Quality Management Systems (QMS) in a pharmaceutical company. It involves defining and operating the QMS health and performance framework, monitoring quality system KPIs, aggregating and trending quality data (Deviations, CAPA, Complaints, Audits), and providing management review inputs to ensure proactive quality checks and inspection-defensible reporting. The role also supports risk-based prioritization and maintains data integrity health signals. While it mentions partnering with tech on QMS data model, AI & Advanced Analytics for quality signals, the core responsibilities are centered on traditional quality systems management and oversight, not AI/ML model development or deployment. | — | 0 |
| Associate Director Government Affairs Associate Director of Government Affairs for a global pharmaceutical company, focusing on representing the company's interests to political decision-makers, associations, and stakeholders at regional, national, and European levels. Responsibilities include building and maintaining political networks, monitoring legislative and regulatory developments, and developing strategic lobbying plans. Requires experience in political parties, ministries, or government affairs within the pharmaceutical sector, and a strong understanding of the German healthcare system. | — | 0 |
| Associate Director - Clinical Development - Neuroscience Associate Director for Clinical Development in Neuroscience at Eli Lilly, focusing on leadership and direction for clinical trials, ensuring high performance, and driving cross-functional collaboration. The role involves business planning, resource management, trial management expertise, and ensuring training and compliance with GCPs and SOPs within a regulated healthcare environment. | — | 0 |
| CMS Intern Intern role focused on planning, implementing, and reporting customer meetings, providing logistical and document management support for congresses and meetings within the healthcare industry. | — | 0 |
| Associate Director - Medical Science Liaison Cardiometabolic Health- Charleston, SC/Savannah, GA The Associate Director - Medical Science Liaison (MSL) for Cardiometabolic Health at Eli Lilly is a field-based role focused on scientific exchange within a specific therapeutic area. The MSL will engage with healthcare professionals to provide and gather in-depth medical and scientific information, acting as a key interface between Lilly and the scientific community. Responsibilities include continuous learning, customer engagement, territory management, and synthesizing customer insights for internal teams. This role requires an advanced degree in health sciences and experience in clinical or therapeutic areas, with a strong preference for cardiometabolic experience. The position emphasizes scientific expertise, strategic thinking, and compliant operations within a regulated healthcare environment. | — | 0 |
| Supply Chain Customer Services Associate The Supply Chain Customer Services Associate at Eli Lilly is responsible for ensuring the best service level in supplying Lilly affiliates, managing the efficient execution of product orders from the Alcobendas plant. This role involves order management, demand planning, logistics coordination, communication with affiliates, participation in improvement projects, and ensuring compliance with established metrics and quality standards. The position also involves participation in digital transformation initiatives related to TMS and eWM. | — | 0 |