Eli Lilly and Company

Project Manager

• Provide project management leadership for the TuneLab machine learning (ML) team
• Partner with engineering to build and maintain the ML development workplan
• Own the ML team's operating cadence end-to-end
• Proactively identify, assess, and escalate risks and issues
• Build and maintain fit-for-purpose processes that improve ML team efficiency
• Drive continuous improvement within the ML team by leading release retrospectives
• Create and maintain operational metrics, dashboards, and reporting frameworks
• Own internal/external partner status updates, surface challenges, resolve/elevate problems

Associate Director, Machine Learning Project Management

Artificial Intelligence

• Support for computational biology workflows, including single cell, spatial, and other multi-omics analysis workflows for clinical and preclinical applications
• Use modern workflow managers (e.g. Nextflow, Snakemake, or similar) and containerization (Docker, Singularity) to make pipelines portable, testable, and reusable across projects and teams
• Help build and maintain reproducible analytical pipelines for statistical genetics and bioinformatics workflows
• Wrap and harden ad-hoc analytical scripts written by scientists into production-quality tools that can be re-run reliably by others
• Write tests, documentation, and clear examples so the pipelines you build are usable by colleagues with a range of technical backgrounds
• Prototype agentic workflows that automate established and routine analytical tasks — for example, pulling target evidence across data sources, generating standardized due-diligence reports, or letting scientists interrogate complex datasets in natural language
• Build and maintain MCP connectors that expose internal data, public resources, and analytical pipelines to LLM-based agents and tools like Claude
• Identify and develop use cases where LLMs and agentic AI workflows can improve the speed, quality, consistency, or accessibility of work across therapeutic areas, focusing on end-to-end capabilities rather than isolated task completion
• Contribute to a shared library of reusable AI tooling, prompt patterns, and integration code that the team can build on.
• Define technical standards for evaluation, documentation, guardrails, and workflow quality so that AI-based solutions are trusted, reproducible, and suitable for repeated use across teams and projects
• Know the latest with the AI tooling landscape and bring back ideas the team can put to work.

Applied Bioinformatics Engineer, Pipelines – AI

Vice President

• Own the global HEOR strategy across the OBU portfolio, from early pipeline through lifecycle management
• Maintain fluency in the global HTA landscape including NICE, G-BA, HAS, CADTH, and other key bodies; proactively advise tumor teams and GPLs on HTA implications for evidence generation strategy
• Facilitate the design, execution, and oversight of HEOR studies including PRO endpoint strategy, health utility studies, indirect treatment comparisons (ITCs), cost-effectiveness models, real-world evidence studies, and burden of illness analyses

Associate Vice President – HEOR – Oncology

Translator

• Supporting laboratory and administrative operations at The Foundry
• Preparing equipment sets and running experiments including initial set-up, sampling and performing basic at-line analyses
• Ordering, staging, and dispensing materials followed by preparation of buffers and solutions for experiments
• Performing basic maintenance of process equipment and supporting infrastructure
• Contributing to process troubleshooting and investigations by supporting process deviations, quality events, and non-conformances

Technician/Sr. Technician/Expert Technician - Process Translation and Execution

QA Engineer

• Provide quality oversight in Analytical testing, namely: molecule and modality support, qualification of new contract labs, audit support, quality system ownership, leading compliance projects for analytical within the Foundry, and quality assessments of quality documentation (e.g., deviations, change records)
• Provide quality oversight of method verification, qualification, and validation activities
• Ensure that appropriate quality systems are in place and are being utilized
• Facilitate quality improvement initiatives, and the implementation of new quality standards
• When necessary, evaluate potential impact of incidents on quality of materials, or the integrity of data
• Ensure appropriate investigations are conducted for deviations, stability failures and out of specification (OOS) results
• Review and approval of the corresponding documentation
• Perform Quality Assurance review and/or approval/rejection of GMP documentation and ensure that review/approval by appropriate technical experts has occurred
• Be available for consultation on quality-related issues as needed
• Network with Lilly quality organizations in the implementation of quality laboratory systems and share best practices
• Promote a positive quality culture and oversee quality presence in the respective laboratory areas
• Identify and lead process improvement projects impacting multiple business areas

Senior Principal Associate – Analytical Quality Assurance

Data Engineer

• Lead the design, development, and delivery of patient analytics data products supporting LillyDirect pharmacy: patient journey tracking, prescription initiation, dispensing fulfillment, and program engagement analytics
• Integrate LillyDirect data flows into the consumer first-party data ecosystem, ensuring patient analytics align with and extend the broader consumer engagement platform and 1PD data standards
• Architect HIPAA-compliant data infrastructure for the LillyDirect platform — including HIPAA authorization capture, SPI consent management, enterprise vs. LillyDirect consent scoping, and revocation propagation across all integrated systems and journeys
• Design and implement tokenization and identity resolution pipelines linking prescription, dispensing, and intake pharmacy partner data to enable end-to-end, privacy-governed patient journey analytics
• Build scalable, reliable data ingestion pipelines for pharmacy partner data (C5/LDP, intake pharmacy feeds); define data quality standards and validation processes for enterprise-scale patient datasets
• Deliver semantic layers and analytics-ready data products — curated datasets, data dictionaries, and governed access patterns enabling downstream BI reporting, self-service analytics, and agentic AI use cases
• Govern data access and privacy controls in coordination with legal, cyber, and privacy teams; own data recertification milestones, Reltio/Cassie integrations, and consent scoping decisions
• Collaborate closely with multi-functional teams — LillyDirect product team, intake pharmacy partners, consumer 1PD analytical platform team, and BIA platform enablement — to translate business requirements into technical specifications and deliver governed, high-quality data products

Associate Director – Data Engineering Lead, LillyDirect Platform

Director

• Identify & Evaluate White Space Opportunities
• Build rapid, credible assessments of unfamiliar markets
• Support all stages of transaction execution
• Manage deal teams and coordinate seamlessly with various departments
• Develop compelling investment cases for presentation to senior leadership audiences
• Maintain a systematic, rolling 18-month catalyst calendar
• Synthesize surveillance intelligence into concise, audience-appropriate outputs

Senior Director – Pharma, Corporate Development & Strategy

Engineer

• The Dry Products Process Engineer role provides technical leadership and support in conjunction with Dry Products External Manufacturing contract manufacturer personnel in the reliable supply and commercialization of medicines with safety first and quality always.
• Developing and sustaining process knowledge to ensure the execution of the appropriate product, process, and operational control strategy at a number of Contract Manufacturers (CMs).
• Direct and Indirect interaction with CM personnel and OEM to ensure reliable supply via the CM execution of the operational control strategy.
• FUME assessment to ensure an understanding of risk presented to the operational control strategy.
• Participation with internal, CM and OEM resources in the equipment specification, procurement, and IQ/OQ/PQ.
• Participation with internal and CM resources to assess the HSE and PSM elements of the CM that impact Lilly products.
• Engaged with internal and external resources in developing capabilities with new or evolving technologies that may impact delivery of internal or external portfolio assets.
• Engage in establishing and sustaining process monitoring for operations on key process equipment, partner with IT/Automation to integrate technology.
• Adherence to the expectations of the Lilly Red Book when carrying out interactions with API EM’s CMs.

Associate Process Engineer – Dry External Manufacturing

Security Operations

• Serve as a member of the Lilly Cybersecurity Identity and Access Management team
• Deliver and secure identity governance technologies that support Lilly's mission
• Partner with business collaborators, IT teams, and cybersecurity colleagues
• Ensure IGA solutions are designed and deployed securely
• Develop technical specifications, design patterns, standards-as-code, and security guidance for identity governance capabilities and services
• Identify and optimize critical processes around identity lifecycle management, access certifications, role engineering, and continuous improvement of IGA technologies

IAM SecOps Engineer – Identity Governance

General Counsel

• Provide strategic, solutions-oriented legal counsel and regulatory and Good Clinical Practice (GCP) expertise in support of Lilly’s clinical development programs
• Serve as the primary legal partner to the Clinical Trials Capabilities team
• Support AI and automation initiatives across clinical development and clinical trial operations
• Provide legal, regulatory, and GCP compliance counsel on R&D Quality matters
• Maintain strong awareness of evolving clinical trial related global drug development expectations and emerging laws, regulations, and guidance
• Influence internal and external collaborators on priority regulatory policy initiatives

Senior Director – Counsel, Clinical Development, Regulatory Legal

Security Engineer

• Evolve one or more AppSec platforms within the Secure SDLC program
• Design and build automation within Security Architecture and Engineering
• Apply LLMs, agentic frameworks, MCP servers, and tool-calling patterns
• Partner with development teams on secure coding practices, threat modeling, and remediation of findings from SAST, DAST, SCA, and secret scanning tools
• Contribute to Lilly's Secure SDLC standards and vulnerability management policy, translating policy into enforceable pipeline and platform controls
• Support the secrets management rollout and migration of applications off legacy secret stores, including code-level guidance for SDK-based and injected consumption patterns
• Produce developer-facing content, reference architectures, secure patterns, short-form instructional content and reusable code samples
• Harden Lilly's CI/CD environment against software supply chain attacks— pinned actions, OIDC-based cloud auth, runner isolation, workflow permissions, and protection of build-time secrets and artifacts
• Partner with the Cloud Security team on Infrastructure-as-Code (IaC) security — extending secure-by-default patterns and developer guardrails from application code into the infrastructure that runs it

Senior Principal Security Engineer, Application Security – Automation

Designer

• The primary responsibilities of the Clinical Design Physician are focused on the design of Phase II to Phase IV clinical programs and studies within the neuroscience therapeutic area.
• Collaborate and complement clinical research staff in the design and conduct of clinical trials
• Understand how design elements influence the ability to deliver on new regulatory expectations
• Support investigator identification and selection, in conjunction with Clinical Development
• Participate in development of scientific data dissemination and preparation of final reports and publications related to assets and/or support efforts to influence clinical design science within the industry

Clinical Design Physician, Neuroscience

• Serve as the subject matter expert in your analytical domain, staying current on innovative methods and making informed recommendations about adoption, adaptation, or development of novel approaches.
• Develop and deploy cutting-edge analytical methods tailored to Lilly's discovery challenges, building workflows that integrate multiple approaches (e.g., physics-based and data-driven) to harness complementary strengths.
• Work alongside discovery project teams to translate complex scientific questions into tractable analytical problems, driving analyses that directly inform compound prioritization, design recommendations, and mechanism of action hypotheses.
• Collaborate with Architecture4Insight to deploy analytical methods as accessible tools and agent-ready capabilities with well-defined APIs for autonomous AI decision-making.
• Identify strategic data gaps in your domain and partner with Scale4Insight to design targeted experiments that generate data in high-value areas.
• Establish best practices for method validation, including prospective testing against experimental outcomes, and demonstrate impact through tracked metrics: decisions influenced, hypotheses generated, and timelines accelerated.
• Collaborate across all Data Foundry pillars and with Frontier AI to ensure analytical capabilities are fully integrated into the broader discovery ecosystem.
• Publish peer-reviewed research, present at scientific conferences, and build analytical literacy across the organization.
• Mentor junior computational scientists and contribute to a culture of scientific rigor, reproducibility, and continuous improvement.

Director, Analytical Methods – Methods4Insight

• Conduct comprehensive medical review of Individual Case Safety Reports (ICSRs)
• Ensure the accuracy, integrity, and compliance of global regulatory reports
• Collaborate cross-functionally and provide technical leadership within Case Management and across Global Patient Safety (GPS)
• Ensure medical validity of ICSRs; Accountable for the review and accuracy of narratives, coding, and assessments of seriousness, expectedness, and company causality
• Complete medical review and follow-up of ICSRs per SOPs for CT and MP cases
• Promptly escalate significant cases and safety issues
• Identify or support evaluation of potential quality issues with Lilly products that may adversely affect patient safety
• Provide training, coaching and mentorship to GPS scientists and physicians with respect to clinical and safety science

Senior Director – Case Management, Medical Review Physician

• Design and implement data models, schemas, and ontologies for chemical, biological, and automation-generated data
• Define and maintain controlled vocabularies, metadata standards, and FAIR-compliant data frameworks
• Implement semantic data standards (RDF, OWL, SPARQL)
• Design and implement data lakehouse architecture using modern platforms (Databricks, Snowflake, or equivalent)
• Build and optimize ETL/ELT pipelines using Spark, dbt, or similar tools
• Implement real-time and streaming data integration (Kafka, Kinesis)
• Design and implement knowledge graphs (Neo4j, Amazon Neptune, TigerGraph)
• Partner with scientific software engineers to ensure data architectures are implementable and performant
• Contribute to build-versus-buy-versus-adopt decisions by evaluating commercial and open-source data platforms