Jobs at Eli Lilly and Company

The Clinical Data Associate will program and test clinical trial data collection systems, collaborate with data analytics teams, and enhance data management processes in trials.

Lead front-line warehouse operations for North American logistics, ensuring safety, cGMP quality, on-time delivery, and cost control. Manage receiving, replenishment, pick/pack/fulfillment, shipments, investigations, CAPAs, staffing, performance management, continuous improvement, and cross-functional coordination across multiple shifts.

Leads oncology brand strategy, digital and omnichannel marketing, customer engagement, promotional campaigns, vendor relationships, and budget management. Develops patient and healthcare professional insights, coordinates cross-functional initiatives with medical, sales, IT, regulatory, and external partners, and measures campaign performance. The role also drives new channel development, digital capability pilots, content localization, and optimization of marketing solutions to improve patient outcomes and commercial performance.

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.

Own the strategy, roadmap, discovery, delivery, and adoption of technical digital products in the pharmaceutical and life sciences domain. Partner with business, engineering, data, scientific, regulatory, and quality teams to translate needs into solutions, manage backlogs, evaluate architecture and technology, track outcomes, and identify opportunities for AI, automation, analytics, and digital innovation.

Leads Lilly’s global corporate social media, digital, and editorial strategy. Builds and manages a high-performing content team, governs owned-channel voice and publishing, develops social campaigns, oversees paid and organic amplification, and connects content performance to reputation and business outcomes. Partners with executive communications, marketing, medical, legal, regulatory, and crisis teams while advancing patient-centric storytelling, AI-enabled workflows, emerging platforms, and global audience engagement.

Leads Kuwait pre-launch and launch preparations for Lilly’s obesity and weight-management portfolio. Develops brand strategy, customer plans, launch readiness activities, stakeholder engagement, and operational tactics. Collaborates with global, regional, and cross-functional teams, manages brand health goals and OPEX, supports thought-leader engagement, and drives environmental shaping and partnership initiatives. Requires strong knowledge of the Kuwait pharmaceutical market and experience in pharmaceutical marketing.

Develop and execute omnichannel brand activation plans for the Italy market, connecting digital campaigns to brand strategy and positioning. Manage personalized audiences and customer journeys through marketing automation platforms, coordinate creative agencies, analyze engagement KPIs, and translate insights into brand recommendations. Collaborate with Italy and Hub-level stakeholders while supporting healthcare brands in an international pharmaceutical environment.

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 complex global learning content projects from initiation through delivery, ensuring timely, budgeted, high-quality outcomes. Builds stakeholder partnerships, translates learning needs into project plans, leads process and technology change, analyzes project data, manages risks, resources, budgets, and vendors, and communicates progress to cross-functional teams. Collaborates with instructional designers, content developers, and technology teams to deploy effective learning solutions globally.

Leads site-wide GMP supply chain, planning, procurement, warehousing, logistics, inventory, master data, and systems support for a new API manufacturing facility. Builds supply chain capabilities and processes during facility startup, ensures regulatory compliance and product availability, manages KPIs and safety stock strategies, coordinates with global supply chain and procurement teams, and supports organizational development, audits, and operational readiness.

Supports Lilly’s Global Operations Strategy Organization through data management, automation, ETL pipeline development, data quality validation, dashboard maintenance, business analysis, process standardization, and AI or machine learning initiatives. The intern will use SQL, Python, VBA, AWS, and Databricks to improve sales force planning capabilities, create insights, document processes, and collaborate with cross-functional stakeholders.

Manage the Suzhou site’s GMARS maintenance system, including asset and maintenance data, work-order planning, scheduling, technical support, training, changes, and deviations. Coordinate preventive and non-emergency maintenance, shutdown scheduling, KPI tracking, data reviews, GECMS support, and QualityDocs approval workflows. Ensure compliance with Lilly requirements, GMP, HSE procedures, and maintenance standards while supporting users and global maintenance teams.

Leads enterprise test automation strategy and delivery, architecting scalable frameworks, writing and reviewing automation code, integrating testing into CI/CD pipelines, and optimizing performance. Defines test strategies, metrics, and quality standards across projects; evaluates emerging and AI-driven testing tools; mentors engineers; and partners with development, DevOps, product, and business teams in Agile environments.

Build and own Lilly’s PR&D semantic layer, ontologies, knowledge graphs, vector retrieval systems, and multi-agent AI architecture. Develop ingestion, triplet engineering, hybrid Graph-RAG retrieval, MCP integrations, orchestration, evaluation, observability, and governance for regulated scientific workflows. Lead technical direction for engineers, mentor teams, partner with science and business stakeholders, own the roadmap, and ensure compliance with GxP, FDA 21 CFR Part 11, privacy, security, and data integrity requirements.

Leads Lilly’s global regulatory writing and study submission capabilities. Develops regulatory writing strategies, training, processes, metrics, and operational excellence across clinical study design and approvals. Advises cross-functional clinical development teams, monitors industry and regulatory trends, represents Lilly in external pharmaceutical forums, and may manage a team of regulatory writing and study development experts.

Leads data engineering strategy, product roadmaps, platform management, KPI frameworks, AI adoption, data onboarding, and access acceleration for Databricks-based lakehouse capabilities. Manages platform reliability, cost, tooling, governance, and lifecycle decisions while directly leading data engineers and product owners. Partners with architecture and business leaders on multi-year direction, facilitates Agile delivery, and promotes reusable data products, self-service access, and AI-assisted engineering across data teams.

Build and own production-grade data pipelines and products across Databricks and AWS lakehouse layers. Conduct mixed-methods research with clinical, scientific, safety, and regulatory users to define data-product requirements. Apply AI-assisted engineering, self-healing automation, observability, CI/CD, and infrastructure as code. Evaluate enterprise platforms, shape technology direction, establish data contracts and governance, mentor engineers, and deliver reliable self-service data products supporting clinical and regulatory workflows.

Manage global Orexin drug development programs across cross-functional teams. Responsibilities include integrated Gantt planning, dependency and risk management, dashboards, governance meetings, budgets, vendor oversight, regulatory submission support, and process improvement. The role requires extensive pharmaceutical or biotech R&D experience, expertise across clinical, nonclinical, CMC, and regulatory development, and strong project leadership skills.