Eli Lilly and Company

Data Engineer

• Drive impact by building the data foundations for People Analytics AI-enabled products and ensuring data readiness for integrated analytics
• Streamline data management, build automated data pipelines, and create data products for People Analytics
• Build, maintain, and manage security pipelines for People Analytics products to reduce compliance risks and ensure controlled access
• Develop People Analytics-specific data products leveraging Python and Microsoft Fabric to enable faster, cleaner, and more reliable data integration into PowerBI
• Build and maintain robust and scalable semantic data models for AI-ready People Analytics dashboards to increase self-service analytics adoption
• Manage continuous People Analytics data updates and automate data pipelines to reduce manual intervention and improve data accuracy
• Partner with HR Technology and Tech@Lilly (IT) to support foundational build and testing of data integration into the HR Enterprise Data Warehouse
• Manage team documentation and business continuity plans

Associate Data Engineer, People Analytics

Director

• Lead a portfolio of external research collaboration project(s)/program(s) with significant risk, financial/resource requirements, and complexity to achieve key objectives
• Develop and implement the operational framework and effectively manage Lilly’s relationship with the external partner to deliver the project's strategic goals
• Manage the complex dynamics and situations that arise in the course of collaborative interactions with external partners; anticipate and resolve issues that would hinder achieving the objectives of the collaboration; coach/advise leaders and team members to address issues; negotiate alignment with the partner’s leaders; make recommendations to management regarding a wide range of business matters related to the partnership
• Establish partnership mission and guiding principles for the alliance and act as an independent ombudsman to lead the team and support the sponsors
• Lead and facilitate alliance governance meetings
• Ensure that Lilly team members discuss relevant corporate policies, processes, and priorities with the partner and help gain alignment on new alliance processes developed (e.g., Compliance, Business Planning, etc.)
• Develop partnership interventions to increase teamwork/trust between Lilly and its partners
• Ensure that integrated, transparent business processes are established between internal and external partners to ensure the teams meet the alliance's stated objectives and goals within contractual obligations
• Drive results across multiple functions and provide recommendations/solutions to improve the effectiveness of Lilly’s external research collaborations
• Proactively identify potential issues/problems and develop mitigation and contingency plans
• Anticipate key decision points and plan for all aspects of developing, forming, managing, and, if necessary, restructuring or terminating alliances
• Provide oversight and accountability for the contract terms related to the alliance; provide input to existing contracts when appropriate; negotiate or modify terms as required
• Provide timely constructive feedback to alliance partners and Lilly personnel concerning their performance in keeping the alliance healthy
• Share key learnings across Lilly regarding the structure of early phase research collaborations to further Lilly’s partnership capabilities

Senior Director – Alliance Management

QA Engineer

• Lead GCP QA activities and establish functional QA procedures for sponsor oversight of internal operations and contracted clinical investigations
• Ensure clinical sites, imaging centers, investigators, and other contracted third parties are qualified and maintained according to risk-based industry standards and study documentation
• Support cross-functional teamwork and provide QA support to Clinical Operations, Imaging Operations, Medical, Statistics, and Avid QA team members
• Work with Global Medical Quality Organization to establish and maintain Avid’s practices with corporate standards and monitor regulatory intelligence for evolving guidelines
• Lead and manage the GCP external audit program including designing procedures for sponsor QA responsibilities and site quality audits
• Oversight and monitoring of investigational sites and third-party organizations
• Establish and provide risk-based quality oversight of GCP external organizations
• Support GCP operations in decisions related to patient safety, efficacy data, product quality, deviation/CAPA management
• Evaluate quality systems, operational controls, facilities, and qualifications/training of personnel of third-party organizations
• Align and implement global QMS standards through internal audits and periodic self-assessments
• Educate Avid personnel on GCP inspection trends and lead continuous improvement efforts
• Ensure adequate procedures, tracking, and reporting systems in alignment with industry standards and corporate policies for GCP document management, change control, deviations/investigations, complaint management, computer systems, data integrity, risk analysis, CAPA, training, audit management, regulatory intelligence
• Lead/support Avid QA efforts in GCP investigations and critical events and escalate significant issues
• Review clinical study protocols for compliance and clinical imaging data accuracy
• Lead GCP Inspection Readiness and support regulatory inspections and/or reviews
• Develop presentation materials for management review of KPIs, regulations, inspection themes, and inspection readiness
• Provide/support GCP QA expertise toward computer systems qualification and validation and ensure contracted third party systems meet regulatory standards
• Coordinate and verify GCP QMS is established and effective from protocol inception through Clinical Study Report completion

Associate Director, Clinical Operations Quality Assurance

• Provide technical leadership for the design, development, and implementation of Lilly’s end-to-end case management capabilities
• Oversee ICSR activities and case quality, including data analysis, trend reporting, KPIs, and business insights
• Manage ICSR vendor and CRO relationships, including process review and remediation
• Define and monitor global ICSR metrics and safety business insights via dashboards
• Drive digital enablement, operational excellence, and integration of new technologies for case management
• Lead global projects on safety systems ensuring strategy, risk management, and continuous improvement
• Prepare for and support regulatory inspections and internal/external audits related to ICSR processes
• Build, mentor and maintain a community of ICSR subject matter experts and recruit/develop team
• Represent Case Management cross-functionally and with external industry groups and partners
• Support the EU QPPV role to enable fulfillment of legal responsibilities

Senior Director – PV Case Management, ICSR

Data Analyst

• Serve as the social listening subject matter expert, providing data-driven insights that meet business objectives
• Provide consultative social listening services and deliver strategic social insights to internal brand and Medical Affairs teams
• Maintain and update queries, ensuring queries for social listening are pulling relevant information and filtering out spam
• Synthesize findings from social media sources; create meaningful insights and clear implications for action
• Incorporate social listening analyses with other customer research, data analysis, and other insight-gathering activities
• Leverage social media listening tools to create timely research and reporting on customer insights, competitive analysis, product insights and emerging trends
• Deliver findings to 6+ Lilly product brands, Medical Affairs partners, and other internal stakeholders
• Create and refine established KPIs for social listening measurement
• Consult for how to best use social listening to reflect brand sentiment, brand health, and overall brand affinity
• Partner with data and analytics team, social strategists, and media services to measure overall performance of social channels
• Collaborate with Community Managers to understand audience engagement with owned content
• Ensure appropriate training, compliance and management of social listening AE/PC reporting and storage of PI across the social listening team and external suppliers
• Research and report on social trends amongst industry and competitors as well as technology and viral social marketing opportunities
• Monitor and apply findings for ongoing development of global platforms on TikTok, Facebook, YouTube, Instagram, and others
• Provide the Customer Experience Hub and business with new ways of thinking about all realms of social media, including content, engagement, data and personalization

Associate / Senior Associate / Manager – Social Listening & Data Analytics

• Architect and implement comprehensive IT strategies across four therapeutic areas, ensuring seamless alignment with scientific priorities and business objectives
• Partner with C-suite and therapeutic area leadership to champion ground-breaking digital initiatives that drive competitive advantage
• Build forward-looking technology roadmaps that anticipate and exceed the evolving needs of modern drug discovery
• Collaborate with scientific partners to define and deliver OMICS data capabilities supporting pre-clinical discovery, including scRNA-seq, spatial transcriptomics, proteomics, CRISPR, and PerturbSeq technologies
• Champion the implementation of FAIR (Findable, Accessible, Interoperable, Reusable) data principles to improve research efficiency and reproducibility
• Design and communicate product vision for therapeutic area-specific data platforms that accelerate the drug discovery pipeline
• Establish scalable, cloud-native infrastructure supporting advanced OMICS data acquisition, processing, and analysis
• Lead high-performing, multidisciplinary teams of bioinformaticians, data scientists, software engineers, and product designers
• Apply Agile methodologies to manage sophisticated product development lifecycles spanning multiple therapeutic areas
• Foster a culture of innovation and collaboration that breaks down silos between scientific and technical teams
• Drive clear, critical communication that synthesizes diverse partner perspectives into unified action
• Cultivate strategic relationships with industry-leading technology partners (DNAnexus, Broad Institute, BioTuring, Illumina) and academic institutions
• Evaluate and integrate emerging technologies and data sources with ground-breaking potential for therapeutic research
• Lead vendor selection and partnership negotiations to enhance value and innovation across the portfolio
• Stay ahead of industry trends to find opportunities for competitive differentiation
• Manage multi-million dollar budgets across direct and indirect IT investments for all four therapeutic areas
• Drive operational excellence through process optimization and continuous improvement initiatives
• Ensure timely delivery of high-impact projects while proactively leading risks and dependencies
• Balance innovation investments with operational stability to increase ROI

Senior Director, Therapeutic Research Technology

Attorney

• Provide legal administrative expertise for global patent application filing, prosecution, and maintenance processes
• Manage patent dockets across patent lifecycle including filing, prosecution, cited reference coordination, formalities, record creation and maintenance, and decision workflows
• Engage with internal and external patent professionals to ensure seamless filing, prosecution, and maintenance of patents and applications
• Anticipate and research complex fact patterns, lead troubleshooting investigations, problem-solve, and produce reliable work product
• Integrate with peers and business units; communicate or escalate barriers or unmet support needs
• Lead small projects or guide complex patent project activities; assist in coordinating resources and serve as a resource to drive progress
• Assess impact of IP industry changes on departmental strategies, policies, and processes
• Engage other resources as needed to fulfill responsibilities
• Employ organization skills and verbal/written interactions with legal colleagues, inventors, business clients, international law firms, vendors, and external parties

Associate - Legal Operations Support

Engineer

• Provide technical leadership and expertise in development, implementation, and maintenance of process safety management and engineering support services for the Lilly Lebanon API site across construction, startup, and operations
• Support development and implementation of the process safety management operational readiness plan for the facility
• Support project team on process safety design decisions, construction, and startup plans ensuring compliance and project deliverables
• Provide oversight and support of process hazard analysis and facility siting studies
• Develop and roll out PSM program elements: employee participation, Management of Change, Pre-Startup Safety Review, Process Hazard Analysis, etc.
• Provide training, mentoring, and onboarding to build a strong process safety culture
• Oversee operations of pharmaceutical API manufacturing units and partner with Operations, Maintenance, and Engineering
• Ensure application of industry codes and standards (e.g., NFPA 30, NFPA 652) and overpressure protection requirements
• Build technical relationships with corporate and site process safety colleagues and network externally (CCPS, P2SAC, ACC)
• Role may begin remotely with occasional travel to Indianapolis HQ and new site area; full relocation to the new site area will be required

Process Safety Engineer

Security Engineer

• Participate in threat modeling sessions and document risks, mitigations, and recommendations
• Consult on security control design and validate effectiveness during system development and testing
• Support security operations and consulting by contributing scripts, automation, or analysis tooling
• Contribute to secure design reviews and provide recommendations to strengthen architecture security
• Partner with developers, infrastructure teams, and architects to embed security early in design and development
• Assist in preparing security documentation, standards, patterns, and knowledge-sharing materials
• Support security assessments and validation of security controls
• Collaborate with senior engineers to learn and apply security frameworks, tools, and best practices
• Communicate findings clearly for both technical and non-technical audiences