Job Description

Job ID: R-110985Company: LillyLocation: Indianapolis, Indiana, United States of AmericaJob Type: Full TimeCategory: Research & DevelopmentPosted Date: 2026-09-11At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Function: Immunology Informatics / Human GeneticsLevel: R5-R6Location: Indy or BostonAbout the RoleThe Immunology Informatics team integrates human genetics into drug discovery and development across the autoimmune disease spectrum (rheumatology, gastroenterology, and dermatology). We are seeking a statistical or population geneticist to strengthen our target identification and validation efforts by applying rigorous quantitative genetics methods — including Mendelian randomization, GWAS interpretation, fine mapping co-localization, and multi-omic integration — to identify, prioritize and de-risk therapeutic targets across the immunology pipeline.This role sits at the interface of human genetics, translational biology, and drug development strategy, working closely with target discovery, translational medicine, statistical, and bioinformatics colleagues, as well as external partners.What You'll DoTarget Evaluation & Genetic Evidence AssessmentLead systematic genetic evidence reviews for existing and emerging immunology drug targets, synthesizing GWAS, exome/whole-genome sequencing, and rare-variant data to assess causal support and directionality (loss-of-function vs. gain-of-function phenotype concordance with therapeutic hypothesis). Build and maintain target evaluation frameworks that score genetic evidence quality, effect direction, and development-stage relevance across a target portfolio.Interrogate and interpret summary and individual levels data from public and licensed genetic resources (e.g., Open Targets, GWAS Catalog, UK Biobank, AllofUs, FinnGen) to support go/no-go and prioritization decisions for drug targetsPropose novel drug targets with strong human causal evidence for autoimmune diseases.Make decision enabling judgements on drug target quality strong scientific rationalePopulation Genetics, Mendelian Randomization, Causal InferenceDesign, execute, and critically evaluate evidence from large population-scale datasets using Mendelian Randomization and other methods to test causal relationships between genetic variamts, biomarkers/proteins and immune-mediated disease outcomes.Assess genetic instrument validity for Mendelian Randomization, pleiotropy, and sensitivity of MR findings (e.g., MR-Egger, weighted median, colocalization) and communicate limitations clearly to immunologists.Collaborate with external genetics partners and academic collaborators on specific genetics programs.Cross-Functional Collaboration & CommunicationTranslate complex genetic and statistical findings into clear, decision-relevant summaries for target discovery teams, translational scientists, and portfolio governance.Contribute genetics-informed input to target nomination packages, competitive intelligence, and program strategy documents.Represent statistical genetics perspective in cross-functional target review forums.Required QualificationsPh.D. in statistical genetics, population genetics, genetic epidemiology, biostatistics, computational biology, or a related quantitative field (or M.D, M.S. with equivalent industry experience).Demonstrated experience working on large-scale population datasets, Mendelian randomization (MR) methodology and causal inference from human genetic datasetsStrong proficiency in R, ideally within a tidyverse-based workflow; comfort with reproducible, version-controlled analysis (Git); basic knowledge of PLINK or other tools to manipulate large genotype datasetsPreferred QualificationsPractical experience interrogating large-scale genetics/genomics databases (e.g. UK Biobank, AllofUS, Open Targets,) and their APIs.Demonstrated proficiency using fine-mapping, and colocalization approaches for GWAS summary statistics to refine association signals and identify causal genetic variants.Ability to critically evaluate statistical/analytical pipelines for genetic analysis and communicate methodological trade-offs to interdisciplinary teamsExperience in immunology/immune-mediated population genetics.Experience integrating multi-omics with genetics data, including pQTL or eqTL analysis.Familiarity with drug target identification/validation criteria and workflows in a pharmaceutical or biotech R&D setting.Experience collaborating with external genetics/data partners or academic consortia.What Success Looks Like in This RoleProviding a defensible, well-documented genetic evidence assessment that underpins target prioritization decisions across the immunology portfolio.Proposing novel targets within the immunology spaceEnsuring that MR and other causal-inference methods are sound, appropriately caveated, and actionable for non-specialist stakeholders.Establishing strong working relationships with target discovery, translational medicine, and external genetics collaborators.Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is$153,000 - $246,400Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.#WeAreLillySkillsmendelian randomizationpopulation geneticsgenetic evidence assessmentgwas interpretationcausal inferencergenome-wide association studiesplinktidyversegenome-wide data analysisgenetic data interpretationstatistical analysisgenetic data miningopen targetsuk biobankallofusfinngenfine-mappingcolocalizationstatistical modelingbioinformaticsdrug target identificationdrug target validationcross-functional collaborationscientific communicationimmunologypharmaceutical r&dexternal collaboration

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