Eli Lilly and Company

Director

• Lead and manage a team of Clinical Research Leads (CRLs and rCRLs; Investigator Engagement Team) within a defined geography
• Collaborate with business partners to ensure clinical trials/studies across all therapeutic areas are executed in accordance with the scientific objectives, country-specific clinical trial strategy, timelines, budget, and local requirements
• Ensure consistent high quality interactions with, and timely robust performance of, global clinical trial sites and vendors
• Responsible for recruitment, training and development of the Investigator Engagement Team
• Ensure on time delivery of database locks within the region/country(ies)
• Provide vendor oversight of delegated responsibilities for site monitoring activities of trial within the country(ies)
• Engage externally with all appropriate bodies to understand country(ies) Clinical Trial regulatory environment(s)
• Manage Country Business planning and execution (Budget/capacity)

Associate Director / Director, Investigator Engagement

Attorney

• Develop and manage eDiscovery SOPs and workflows across the EDRM spectrum, ensuring best practices, defensibility, and efficiency at each stage.
• Partner with various business areas on processes to preserve data per legal hold requirements, including automated workflows and guidance on evolving technologies, data migrations, and system retirements.
• Develop and manage data collection processes from various enterprise systems and data sources/lakes, ensuring proper metadata overlays as needed and chain-of-custody documentation.
• Manage acquisition integration, including legal holds, data collection, and data migration into Lilly’s systems.
• Provide eDiscovery guidance to business and technology teams regarding preservation of data and defensible collection processes.
• Oversee processing, hosting, and review platforms and workflows.
• Evaluate and implement eDiscovery tools and technologies to enhance operational capabilities and efficiencies, including automated workflows and data collection.
• Drive adoption of AI and machine learning solutions, including technology-assisted review, predictive coding, advanced analytics, and AI.
• Stay current with emerging technologies and industry trends to inform strategic direction.
• Contribute to the strategic vision and roadmap for Lilly's eDiscovery program.
• Manage eDiscovery vendors, with a focus on evolving technology to inform the roadmap.
• Mentor and develop team members, fostering growth and technical expertise.
• Effectively collaborate to drive solutions with cross-functional teams including Legal, Privacy, Records Management, Information Technology, Compliance, Security, and various Business Units.

Associate Director – Legal eDiscovery

Full-stack Engineer

• Work with laboratory scientists to develop new features and enhance existing functionality for workflow management, including assay request handling, plate definitions, and sample tracking and results analysis
• Maintain and extend integrations with internal / external APIs
• Design, implement and test database schema changes, write efficient queries for PostgreSQL
• Write unit tests, integration tests, and ensure code coverage
• Demonstrate best practice on code quality, documentation, CI/CD rigor, and architectural best practices, ensuring our research code is robust enough for enterprise production.
• Serve as a bridge between discovery teams, and IT/Cloud organizations, converting scientific intent into rigorous engineering specifications.

Software Engineer

• Define and drive the DDCS delivery system innovation strategy, establishing the vision, priorities, and sourcing mix (internal and external) for the early-phase pipeline in alignment with Lilly’s therapeutic and commercial objectives.
• Build and lead Lilly’s external delivery system innovation ecosystem—forging strategic relationships with academic institutions, venture-backed startups, technology accelerators, CDMOs, and device partners to access and in-license best-in-class delivery technologies ahead of the industry.
• Establish and own the governance framework, stage-gate criteria, and investment decision process for the DDCS early innovation portfolio, ensuring disciplined, data-driven advancement from ideation through proof-of-concept and into formalized development.
• Provide strategic counsel to DDCS senior leadership and the broader Device organization on external innovation trends, competitive landscape, emerging technologies, and portfolio gaps; translate insights into actionable investment theses.
• Champion a culture of innovation and external curiosity across DDCS, building organizational capability in technology scouting, opportunity assessment, and cross-sector collaboration.
• Accountable for the overall health, prioritization, and performance of the DDCS early-phase development portfolio—setting direction for program leads and ensuring alignment between portfolio investments and strategic priorities.
• Integrate portfolio intelligence across internal programs and external partnerships into a unified, leadership-ready view of pipeline status, resource requirements, risks, and investment opportunities for annual business planning and capital allocation.
• Drive DDCS-wide adoption of standardized early development processes, governance frameworks, and innovation metrics, institutionalizing best practices across internal and externally sourced programs.
• Serve as an interface with Lilly enterprise functions—Global Business Development, Corporate Strategy, Research, and Therapeutic Business Units—to ensure alignment between delivery system innovation and drug development priorities.
• Represent DDCS at external conferences, industry consortia, and partner forums; build Lilly’s reputation as a preferred innovation partner in the delivery system and drug-device combination space.
• Influence resource allocation, organizational design, and capability investment decisions within DDCS in support of early-phase innovation strategy.

Senior Director – Early Development Portfolio and Platform Lead

• Serve as the HCI Lead for an assigned Business Unit, partnering closely with BU Medical Affairs and other relevant stakeholders to identify priority customer and care gaps aligned to BU strategy and healthcare system need.
• Lead the strategy, design, implementation, management, and scale-up of collaborative non-grant healthcare improvement initiatives for the assigned BU.
• Support the impact of grant-supported HCI initiatives by identifying opportunities for scale-up, broader dissemination, publication, and practical application where appropriate.
• Ensure HCI initiatives are designed with clear objectives, meaningful implementation and outcome measures, and a focus on measurable impact for patients, providers, and healthcare systems.
• Help identify where healthcare improvement approaches are most likely to create meaningful change in care delivery, patient outcomes, provider behavior, or healthcare system performance.

Executive Director – Healthcare Improvement Hub, Global Implementation Science Specialist, Physician (MD)

• Program and test clinical trial data collection databases
• Collaborate with cross-functional teams to deliver standardized data collection methods
• Lead projects with high complexity and ensure successful implementation
• Support submission and regulatory response activities
• Develop and apply innovative solutions to improve processes

Clinical Study Build Programmer

Product Manager

• Contribute to and help drive the product strategy, roadmap, and vision for computational drug design and optimization platforms
• Deeply understand how computational biologists design, execute, and iterate on multi-objective optimization (MOO) campaigns for therapeutic candidates
• Identify and prioritize opportunities to integrate agentic AI capabilities into discovery workflows
• Establish and track key metrics to measure product success, adoption, and scientific impact
• Work as part of a cross-functional product team with engineering, computational biology, and research stakeholders to translate complex scientific requirements into clear product specifications

Director, Software Product Management – Discovery Research Platforms

• Co-develop and continuously evolve LGL programs by defining the partnership model, operating cadence, and success metrics for resident biotechs.
• Lead external search, validation, and selection of high-synergy biotechs across assigned geographies, and connect companies to Catalyze360 services and Lilly SMEs to address scientific and technical needs from discovery through development.
• Demonstrate drug development leadership and apply deep mechanism-to-disease translation capability through hypothesis generation, study design, and rigorous data interpretation.
• Integrate multiple scientific disciplines and translate across functions by mobilizing internal and external experts and an established industry network to progress biotech scientific plans.
• Build development scenarios across therapeutic areas by anticipating funding, timelines, and value inflection points shaped by VC/biotech dynamics.
• Position and advocate Lilly Gateway Labs externally to attract and recruit top resident companies.
• Provide strategic oversight to the LGL portfolio to accelerate company progress, ensuring clear objectives, milestones, and decision-ready updates.
• Influence and build relationships across diverse internal and external stakeholders in a largely virtual model, demonstrating strong cultural sensitivity across countries and company cultures.
• Model Lilly values through high standards in science and people leadership by setting priorities, coaching and aligning teams, constructively managing conflict, and exercising sound business judgment to represent the enterprise portfolio view.

Senior Director, Gateway Labs

• Serve as the Discovery PKPD project leader for genetic medicines programs, including ASOs, siRNA, LNP-mediated delivery, gene therapy (AAV and non-viral vectors), and antibody-siRNA conjugates (ARC)
• Develop and implement modeling strategies that enhance decision-making for genetic medicines inform translational research strategies
• Design, analyze, and interpret quantitative pharmacology and PK/PD studies
• Collaborate effectively with scientists within and outside the functional area to integrate PK/PD into team strategy and contribute to project team discussions, guiding key go/no-go decisions with quantitative approaches
• Communicate quantitative findings both internally and externally through scientific publications, conference presentations, and cross-functional forums
• Mentor junior scientists and contribute to the growth of PKPD modeling capabilities within the genetic medicines space and neuroscience space

Director – Discovery PKPD Project Leader, Novel Modalities

Artificial Intelligence

• Design and implement AI agents for scientific document authoring, including literature synthesis, citation management, and figure/table generation
• Build retrieval-augmented generation (RAG) systems over scientific corpora, ELNs, and internal knowledge bases to ground AI outputs in factual content
• Develop domain-specific fine-tuning and prompt engineering strategies for chemistry, biology, and pharmacology content
• Create tools for automated quality checking: scientific accuracy, consistency, formatting compliance, and plagiarism detection
• Build multi-agent workflows that coordinate literature search, data extraction, drafting, and revision cycles
• Build production-grade authoring applications with robust software engineering practices (version control, testing, CI/CD)
• Deploy scalable services on cloud-native infrastructure (Kubernetes, AWS) with appropriate guardrails for scientific content
• Partner with scientists, medical writers, and regulatory teams to integrate AI authoring tools into real workflows
• Represent Frontier AI in internal forums and external AI/NLP research communities
• Evaluate external vendors, open-source tools, and academic collaborations for scientific authoring capabilities

Engineer – Scientific Authoring, Frontier AI

• Scientific and Clinical Experts (SEs/CEs) are individuals who are noted for their expertise in a therapeutic area and as a result have special needs for in-depth and cutting-edge scientific information
• Facilitate scientific exchange between industry and the scientific and clinical communities
• Provide leading researchers and effectively synthesize and communicate actionable customer/clinical insights to internal Lilly Medical and cross functional teams
• Use good judgement in decision-making and practitioners with the scientific and clinical knowledge that most meaningfully and precisely addresses their needs
• Establish themself as a reliable, trusted resource of unbiased, accurate, up-to-date, medical and scientific information
• Connect SEs/CEs with other Lilly resources or internal business partners as appropriate and facilitate collaborative research opportunities

Associate Director – Medical Science Liaison, Cardiometabolic Health

Account Executive

• Apoyo en la gestión de cuentas de manera integral entre diferentes especialidades asegurando el flujo de pacientes dentro de un territorio de ventas asignado, identificando oportunidades de crecimiento y maximizando la penetración de nuestro producto.
• Desarrollar conocimiento sobre el mapeo de influenciadores externos (quién refiere, quién decide) para asegurar un diagnóstico temprano y preciso de pacientes susceptibles de tratamiento.
• Colaborar en la planificación basada en insight, con información de múltiples fuentes para diseñar y ejecutar planes de cuenta efectivos y de impacto.
• Visitar regularmente a médicos y otros profesionales de la salud para presentar información sobre nuestros productos, responder a sus preguntas y proporcionar soporte científico.
• Aprender a reportar de forma precisa y oportuna la actividad de ventas y las tendencias del mercado utilizando los sistemas de la compañía.
• Colaborar con otros departamentos de la empresa, como marketing, departamento médico y acceso, para asegurar el éxito de las estrategias comerciales.

Junior Sales Representative

• Serve as scientific lead for programs, driving target identification/maturation
• Design and coordinate implementation of assays and models for drug discovery
• Provide mentoring and performance management to junior scientists
• Communicate and work effectively in a team environment

Director – Scientific Lead, Women's Health

Clinical Research

• The Clinical Research Lead (CRL) is a strategic, field-based scientific leader responsible for driving the execution of Lilly clinical trials through exceptional investigator engagement and site performance management
• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc
• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
• Drive inspection readiness as a continuous discipline across sites
• Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
• Provide oversight and quality assurance for vendor monitoring, escalating risks proactively
• Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer

Associate Director – Clinical Research Lead, Oncology

• Provide medical oversight and strategic leadership throughout the clinical trial lifecycle, including the design, planning, execution, and interpretation of trials for investigational compounds, ensuring patient safety and scientific integrity.
• Contribute to the design and development of key clinical documents, including study protocols, investigator’s brochures, informed consent documents, and other essential materials.
• Ensure the clinical development strategy adheres to industry best practices and regulatory guidelines while collaborating with study investigators and medical experts in the development and execution of study protocols.
• Lead the review and interpretation of clinical trial data, including safety assessments, efficacy endpoints, and overall trial progress.
• Serve as a key medical expert in cross-functional discussions, including regulatory submissions, investigator meetings, and advisory boards.
• Work with the Clinical Operations team to identify and resolve trial-related issues, ensuring smooth execution and compliance.
• Collaborate closely with the clinical operations, regulatory, and data management teams to ensure timely and high-quality execution of clinical trials.
• Collaborate with the research team to develop and implement a translational biomarker strategy for the program integrating early-phase data to inform clinical strategy.
• Contribute to regulatory submission efforts by providing clinical insight into IND submissions, clinical trial applications, and other regulatory documents support responses to health authorities and ethics committees.
• Represent the company at scientific conferences, advisory boards, and meetings with regulatory authorities.
• Develop and maintain relationships with external stakeholders, including key opinion leaders (KOLs), clinical investigators, and contract research organizations (CROs).
• Foster a collaborative and positive team environment that encourages innovation, scientific rigor, and high-performance standards.
• Travel to clinical sites, conferences, and regulatory meetings as needed.
• Other duties as assigned.