Eli Lilly and Company

Compliance

• Provide strategic, tactical, and operational regulatory CMC support across therapeutic modalities and manufacturing technologies
• Support clinical trials, market registrations, and post-approval activities
• Apply CMC technical knowledge and regulatory expertise to develop and execute global regulatory strategies
• Ensure internal consistency, effective change management, and predictable regulatory outcomes
• Build productive relationships across research, development, manufacturing, quality, regulatory, and partner organizations
• Apply technical knowledge of CMC drug development and pharmaceutical manufacturing sciences across drug substance, drug product, and analytical areas
• Develop, implement, and maintain global CMC regulatory strategies
• Provide regulatory advice for development, manufacturing, and lifecycle planning decisions
• Evaluate regulatory impacts, identify risks, and develop mitigation options
• Lead preparation, review, and finalization of CMC documents for global regulatory submissions
• Resolve technical or operational issues affecting submission timing, regulatory compliance, or product supply
• Manage complex issues and propose risk-based regulatory solutions
• Build relationships across regulatory, research and development, manufacturing, quality, and regional teams
• Provide regulatory guidance and subject matter expertise to CMC teams
• Mentor and serve as a resource within the regulatory CMC community
• Incorporate regulations and guidance into processes, tools, templates, and training materials
• Contribute to internal policy development and discussions on emerging regulatory trends
• Participate in industry forums or working groups
• Lead or support cross-functional teams developing and executing global CMC regulatory strategies
• Review CMC development strategies, control strategies, and submission content
• Collaborate with manufacturing sites, technical experts, and quality organizations
• Support health authority interactions, briefing materials, and responses to questions
• Communicate regulatory strategies, risks, and recommendations to stakeholders
• Share regulatory knowledge, lessons learned, and best practices
• Contribute to corporate positions and responses to proposed agency regulations and guidelines

Advisor, Senior Advisor – Regulatory CMC

Designer

• Design Phase II to Phase IV clinical programs and studies in neuroscience
• Translate therapeutic-area and asset-team strategy into clinical development programs and trial options
• Represent program and trial design options to asset teams and senior leaders
• Provide medical and clinical input into study protocols with cross-functional partners
• Assess how protocol features affect feasibility, value, patient and investigator burden, and execution efficiency
• Contribute to asset strategy, portfolio clinical strategy, and asset-specific clinical plans
• Collaborate with clinical research staff on trial design and conduct, including sample size, timelines, grants, and governance reviews
• Review risk profiles and ensure appropriate communication of risks to study subjects
• Support investigator selection, participant recruitment and retention, and transition from design to execution
• Maintain collaborations with external experts, thought leaders, professional societies, conferences, consortia, and the medical community
• Support scientific data dissemination, final reports, publications, and clinical design science
• Evaluate medical literature, competitive products, and scientific developments
• Identify and share best practices for program and protocol design
• Help evolve Lilly standards, tools, processes, templates, and best practices

Clinical Design Physician, Neuroscience

Product Manager

• Define and support the future-state vision and roadmap for consumer companion apps
• Prioritize investments based on consumer impact, health outcomes, and business goals
• Analyze research and data to extract insights and influence product and strategic direction
• Foster a collaborative, team-first product culture
• Manage internal and external partner relationships, scopes, timelines, quality, and roadmap commitments
• Collaborate with design, engineering, user research, business analysts, and product owners
• Champion consumer needs in product decisions using research, usage data, and qualitative insights
• Advocate for intuitive, accessible, and high-quality app experiences
• Provide input on requirements, workflows, designs, features, build, and testing
• Establish technical standards and scalable, modular solutions
• Communicate app performance, strategic direction, and improvement opportunities to stakeholders and senior leadership
• Serve as internal subject matter expert on consumer companion app best practices
• Define and track in-market KPIs with data and analytics teams
• Depending on skills and interests, oversee UAT, launch execution, and/or research and data functions

Director – Associate Director, Product Management, Consumer Apps

Scientist

• Provide strategic insight and leadership into health outcomes evidence needs for Lilly’s portfolio
• Use health outcomes discipline knowledge, therapeutic area knowledge, drug development and commercialization understanding, and geographic market knowledge
• Own and execute research projects
• Develop and articulate product value propositions, patient reported outcomes strategies, real world evidence generation, and differentiation strategies
• Drive sustained integration of HEOR from early clinical development through commercialization
• Develop and oversee health outcomes research strategy for compounds in Lilly’s portfolio
• Serve as a strategic partner on lead/core teams throughout development and/or commercialization
• Formulate and drive Patient Focused Outcome, Real World Evidence, and/or economic value strategies for priority products and geographies
• Develop high-impact science across the product lifecycle to support evidence needs and improve patient outcomes
• Apply technical expertise in statistical analysis, economic modeling, clinical trials, patient-focused outcomes, observational/epidemiologic research, and health technology or value assessment
• Apply disease-state knowledge and research methods to address registration, pricing, reimbursement, and access issues
• Build strategic relationships with internal and external decision makers
• Lead health outcomes evidence planning and implementation with cross-functional teams
• Influence business partners and external stakeholders to achieve goals and outcomes
• Communicate health outcomes information to internal partners, the scientific community, and customers
• Lead dissemination efforts including abstracts, posters, podium presentations, promotional materials, and manuscripts
• Drive application of results and deliverables to increase the impact of health outcomes work
• Monitor developments in portfolio disease states, health outcomes methodologies, market needs, and environmental factors
• Ensure projects meet timelines, budget, and scope by coordinating with cross-functional partners and external collaborators

HEOR Asset Scientist – Advisor

Advisor

• Support evidence generation across the HEOR portfolio
• Contribute to comparative effectiveness and pharmacoepidemiologic studies, systematic literature reviews and meta-analyses, and cost-effectiveness or budget impact modeling
• Design and execute observational studies
• Support quantitative evidence synthesis
• Contribute to development or critique of decision-analytic models used in HTA and payer submissions
• Provide strategic insight and leadership into health outcomes evidence needs for Lilly’s portfolio
• Develop and articulate product value propositions, patient reported outcomes strategies, real world evidence generation, and differentiation strategies
• Drive integration of HEOR from early clinical development through commercialization
• Develop and oversee health outcomes research strategy for compounds in relevant therapeutic areas
• Serve as strategic partner on lead/core teams throughout development and/or commercialization
• Formulate and drive patient-focused outcome, real world evidence, and/or economic value strategies
• Apply technical expertise in statistical analysis, economic modeling, clinical trials, patient-focused outcomes, observational/epidemiologic research, and health technology or value assessment
• Apply disease state knowledge and research methods to address registration, pricing, reimbursement, and access initiatives
• Lead health outcomes evidence planning and implementation with cross-functional teams and external stakeholders
• Communicate health outcomes information to internal partners, the scientific community, and customers
• Lead research dissemination through abstracts, posters, presentations, promotional materials, and manuscripts
• Ensure health outcomes projects meet timelines, budget, and scope
• Maintain awareness of developments in disease states, health outcomes methodologies, and market needs

HEOR Advisor, Methods

Software Engineer

• Program and test clinical trial data collection databases, including mapping, testing, and normalization into a clinical data warehouse
• Configure clinical data collection systems such as eCOA/EDC platforms
• Build study forms, logic, edit checks, workflows, integrations, and data repository mappings
• Gather and influence eCOA design specifications and support implementation
• Understand study translation needs and enable localization
• Deliver accurate data collection systems and data warehouse mappings aligned with study objectives
• Provide insights into study design and data delivery, including the Data Management Plan, Project Plan, database, and observed datasets
• Support submission, inspection, and regulatory response activities
• Lead complex cross-Business Unit/Therapeutic Area projects or programs
• Develop and test innovative solutions
• Improve development speed, accuracy, consistency, and study build cycle time
• Enable metrics reporting for study development timelines and database changes
• Partner with Data and Analytics colleagues to deliver study databases before first patient visit
• Influence data standard decisions and strategies
• Apply regulatory and privacy requirements to study database building
• Integrate multifunctional, external, and technical information for data-driven decisions
• Reduce postproduction changes through change-control processes
• Anticipate and resolve technical, operational, and business problems affecting Data and Analytics
• Manage delivery risks and define database solutions and timelines for the portfolio

Clinical Study Build Programmer

General Counsel

• Serve as Lilly's dedicated regulatory legal lead for its infectious disease and vaccines portfolio and support other emerging therapeutic areas
• Provide day-to-day and strategic legal counsel on vaccine-specific regulatory pathways globally
• Extend regulatory legal support to additional emerging therapeutic areas as assigned
• Lead regulatory legal strategy for interactions with global health authorities, including regulatory issues, inspections, enforcement matters, dispute resolution, and significant agency engagements
• Advise on advisory committee strategy and immunization policy dynamics, including ACIP
• Monitor evolving laws, regulations, and guidance applicable to vaccines and biologics
• Partner with senior leaders across Clinical Development, Regulatory Affairs, Manufacturing & Quality, Patient Safety, Commercial, Policy, and Legal
• Lead regulatory legal workstreams for integration of newly acquired assets and platforms
• Build and scale the regulatory legal capability, including governance models and external counsel strategy
• Lead implementation and execution of regulatory legal support across clinical development, pharmacovigilance, and manufacturing/quality
• Deliver integrated legal guidance to key functions in a complex, matrixed environment

Associate Vice President – Assistant General Counsel, Infectious Disease & Vaccines, Regulatory Legal

Engineer

• Partner with Process Translation and Analytical Laboratories functional areas and site, group, and global IT teams
• Implement and support digital laboratory solutions for the Foundry’s operational objectives
• Drive and support system design, configuration, validation, and release
• Serve as an IT subject matter expert for analytical laboratory IT systems
• Lead system design and configuration sessions for LIMS, LES, ELN, and CDS platforms
• Translate business and scientific processes into validated technical solutions
• Develop and implement IQ, OQ, and PQ protocols in compliance with 21 CFR Part 11 and EU Annex 11
• Lead data integrity requirements and ensure audit readiness
• Coordinate instrument integration and data flows between lab equipment and LIMS/LES platforms
• Support deployment and upgrades of analytical laboratory IT systems
• Produce and maintain CSV documentation, SOPs, and validation plans
• Ensure systems remain validated through releases, recapitalization, and retirement
• Ensure solution requirements comply with regulatory, legal, and quality requirements
• Collaborate with site and global IT teams to ensure operational readiness
• Organize and educate peers on system use and best practices
• Support audits and provide oversight for management reviews, laboratory metrics, equipment records, and laboratory documentation

Principal Informatics Engineer

Director

• Own the engagement strategy and enablement capability for Lilly's cardiometabolic digital influencer stakeholder ecosystem
• Turn external signals into recommendations, practical frameworks, and cross-functional action
• Map partnerships and touchpoints with Digital Opinion Leaders and identify appropriate uses
• Ensure engagement respects Digital Opinion Leaders' independence and educational mission
• Identify ascending digital voices and define effective engagement practices
• Oversee stakeholder engagement utilization strategy across verticals
• Define identification and prioritization criteria with Ecosystem Intelligence, AI, and Technology leads
• Provide recommendations on which stakeholders to engage and where to focus efforts
• Build connectivity to top global stakeholders and maintain strategic relationship oversight
• Design, pilot, evaluate, and scale new engagement approaches
• Develop frameworks, toolkits, playbooks, and operating guidance with compliance guardrails
• Design and deliver training; provide coaching and hands-on support
• Draft stakeholder communications and support executive engagement preparation
• Track engagement outcomes against relationship, insight, co-creation, and practice-impact metrics
• Report results and improvement recommendations to the Engagement Strategy lead and cross-functional partners
• Partner with U.S. and IBU affiliates to align stakeholder needs and best use
• Track activities and stakeholder utilization against strategic plans and requirements

Associate Director – Digital Opinion Leader, Cross-Stakeholder Enablement Lead

Account Manager

• Lead engagement with the early-stage drug discovery community, including startups, established biotechs, mid-cap pharma, VCs, and emerging model developers
• Serve as the primary interface for TuneLab user activation, feedback, and early-stage partnerships
• Shape strategies to grow TuneLab and expand the platform’s reach
• Develop and execute strategies to identify, attract, and activate biotech users and contributors
• Build frictionless onboarding mechanisms, including self-service tools, community forums, and scalable support
• Design and implement user activation programs such as training sessions, demo days, and working groups
• Build repeatable collaboration models for biotech startups, academic groups, and mission-driven organizations
• Collaborate with product and technology teams to ensure contribution processes are technically feasible and supported
• Serve as the first point of contact for inbound interest from biotechs, labs, and researchers
• Qualify and prioritize leads based on platform strategy and scientific fit
• Collaborate with legal, product, and technical teams to formalize engagements and support execution
• Support TuneLab partners to ensure technical success
• Build partner case studies and champions demonstrating TuneLab’s impact on biotech companies
• Identify product improvements from partner discussions and share them with the Product team
• Represent the platform at scientific meetings, AI/ML community gatherings, and academic events
• Build visibility through storytelling, case studies, and public programming
• Cultivate identity and shared purpose among ecosystem participants

Senior Director – Ecosystem Growth, Contributor Partnerships

• Lead engagement with the early-stage drug discovery community, including startups, established biotechs, mid-cap pharma, VCs, and emerging model developers
• Serve as the primary interface for TuneLab user activation, feedback, and early-stage partnerships
• Shape strategies to grow TuneLab and expand its reach
• Develop and execute strategies to identify, attract, and activate biotech users and contributors
• Build frictionless onboarding mechanisms, including self-service tools, community forums, and scalable support
• Design and implement user activation programs such as training sessions, demo days, and working groups
• Build repeatable collaboration models for biotech startups, academic groups, and mission-driven organizations
• Collaborate with product and technology teams to ensure contribution processes are technically feasible and supported
• Serve as the first point of contact for inbound interest from biotechs, labs, and researchers
• Qualify and prioritize leads based on platform strategy and scientific fit
• Collaborate with legal, product, and technical teams to formalize engagements and support execution
• Support TuneLab partners to ensure technical success
• Build partner case studies and champions demonstrating TuneLab’s impact on biotech companies
• Identify product improvements from partner discussions and share them with the Product team
• Represent the platform at scientific meetings, AI/ML community gatherings, and academic events
• Build visibility through storytelling, case studies, and public programming
• Cultivate identity and shared purpose among ecosystem participants

• Own the engagement strategy and enablement capability for Lilly's CMH digital influencer stakeholder ecosystem
• Turn external signals into clear recommendations, practical frameworks, and cross-functional action
• Understand partnerships and touchpoints with Digital Opinion Leaders and map best practices and appropriate use
• Ensure engagement with Digital Opinion Leaders respects their independence and educational mission
• Identify ascending digital voices and define effective engagement approaches
• Oversee stakeholder engagement utilization strategy across all verticals
• Understand and triangulate stakeholder preferences, business strategies, and compliance requirements
• Define identification and prioritization criteria with Ecosystem Intelligence and AI & Technology leads
• Translate DOL stakeholder insights into recommendations on engagement priorities
• Build connectivity to top global stakeholders and maintain strategic relationship oversight
• Serve as internal expert on effective engagement with stakeholder types
• Design, pilot, and evaluate new engagement approaches
• Codify successful pilots into scalable frameworks, playbooks, and operating guidance
• Scan the external environment for innovative engagement models and emerging best practices
• Develop and maintain engagement frameworks, toolkits, and playbooks
• Embed compliance guardrails and accountability standards into frameworks
• Design and deliver stakeholder-category training
• Provide coaching, guidance, and hands-on support for teams applying frameworks
• Draft key stakeholder communications
• Support executive engagement preparation by identifying new stakeholders and opportunities
• Track engagement outcomes against metrics including relationship depth, insight quality, co-creation output, and practice impact
• Report results and improvement recommendations to the Engagement Strategy lead and cross-functional partners
• Build and implement cross-functional stakeholder utilization strategy
• Partner with U.S. and IBU affiliates to align stakeholder needs and best use
• Manage lists of highly utilized stakeholders and ensure teams understand use cases
• Collaborate with a project manager to track activities against strategy and utilization requirements/cap

Machine Learning Engineer

• Build and maintain end-to-end ML deployment pipelines, including experiment tracking, model versioning, containerized model serving, and automated retraining triggers
• Develop model registry infrastructure and feature engineering pipelines
• Implement monitoring and alerting for data pipelines, APIs, ML models, and agentic systems
• Build dashboards and metrics for pipeline execution, API latency, token usage, prediction quality, and system health
• Establish structured logging and tracing infrastructure
• Deploy predictive and analytical methods in cheminformatics, structural biology, bioinformatics, and reaction informatics
• Build serving infrastructure for synchronous, asynchronous, batch, and agent-invoked workloads
• Define API contracts, documentation standards, and testing frameworks
• Build and operate cloud-native model-serving infrastructure using containers, Kubernetes, and infrastructure-as-code
• Develop CI/CD pipelines with automated validation, A/B testing, canary deployments, and rollback procedures
• Integrate model serving with Data Foundry data pipelines
• Partner with Frontier AI and Tech@Lilly to expose scientific tools through REST APIs and MCP-compatible endpoints
• Collaborate on API latency, throughput, and graceful-degradation requirements
• Work with Methods4Insight scientists to implement uncertainty quantification and confidence metrics

Engineer – MLOps, Scientific Platforms

Sales

• Fortalecer la habilidad como consultor y ampliar la experiencia y visión de negocio en mercados Privado y Gobierno
• Generar demanda y acelerar el crecimiento en mercados de Oncología, privado e instituciones del sector salud federal y estatal
• Obtener acceso y gestionar procesos de compra en Instituciones Descentralizadas, IMSS e ISSSTE
• Buscar constantemente y desarrollar nuevos negocios en el mercado Privado y Descentralizados
• Interactuar con Thought Leaders del mercado de oncología

Sales Representative, Oncology

• Fortalecer la habilidad como consultor y ampliar la experiencia y visión de negocio en mercados privado y de gobierno
• Generar demanda y crecimiento acelerado en mercados de Oncología, privados e instituciones de salud federales y estatales
• Obtener acceso y gestionar procesos de compra en instituciones descentralizadas, IMSS e ISSSTE
• Buscar constantemente y desarrollar nuevos negocios en mercados privados y descentralizados
• Trabajar con una base en Ciudad de México y viajar a Chihuahua, Ciudad Juárez, Tampico y Toluca

Advisor, Senior Advisor – Regulatory CMC

Clinical Design Physician, Neuroscience

Director – Associate Director, Product Management, Consumer Apps

HEOR Asset Scientist – Advisor

HEOR Advisor, Methods

Clinical Study Build Programmer

Associate Vice President – Assistant General Counsel, Infectious Disease & Vaccines, Regulatory Legal

Principal Informatics Engineer

Associate Director – Digital Opinion Leader, Cross-Stakeholder Enablement Lead

Senior Director – Ecosystem Growth, Contributor Partnerships

Senior Director – Ecosystem Growth, Contributor Partnerships

Associate Director – Digital Opinion Leader, Cross-Stakeholder Enablement Lead

Engineer – MLOps, Scientific Platforms

Sales Representative, Oncology

Sales Representative – Oncology