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Applied AI Engineer, Clinical Informatics
Eli Lilly and Company. Develop and deploy agentic AI applications enabling natural-language interaction with clinical data .
Posted 10/5/2026full-timeBoston • Massachusetts • United StatesMid-LevelSenior💰 $166,500 - $266,200 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and deploying AI applications for clinical data analysis, utilizing advanced statistical modeling, machine learning, and natural language processing techniques. Proficient in managing clinical trial datasets and ensuring compliance with relevant regulations such as HIPAA and GDPR.
Highest-signal resume keywords
Expert Proficiency In PythonExpert Proficiency In RStrong Command Of SQLExperience With SDTM/ADaMDemonstrated Use Of AI Tools In Production Environments
ATS Keywords
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Hard Skills
Statistical ModellingMachine LearningNatural Language ProcessingSurvival AnalysisCausal InferenceDeep LearningMulti-Omic Data AnalysisKnowledge Graph ConstructionGraph MLOntology-Driven Reasoning
Tools & Technologies
DNAnexusAWSGCPAzureHPC Clusters
Industry Keywords
Biomedical InformaticsComputational BiologyBioinformaticsStatistical GeneticsEpidemiologyClinical Trial DataBiobank DataHIPAA ComplianceGDPR ComplianceIRB Requirements
Tech Stack
Tools & technologiesAWSAzureCloudGoogle Cloud PlatformPythonSQL
About the role
Key responsibilities & impact- Develop and deploy agentic AI applications enabling natural-language interaction with clinical data
- Ground AI outputs in validated biological knowledge using RAG pipelines anchored in biomedical ontologies, clinical trial registries, and curated pathway databases
- Deploy unsupervised and self-supervised learning to discover latent patient archetypes and molecular disease subtypes across trial and biobank data
- Deploy survival models and dynamic treatment regime estimators using combined clinical and omics features
- Harmonize heterogeneous trial and biobank datasets to common data representations
- Evaluate and monitor model performance, safety, and reliability in production environments
- Manage vendors, contractors, and partner relationships across Lilly
- Build pipelines for locked clinical trial databases using SDTM and ADaM for secondary and exploratory research
- Identify trial subgroup effects, treatment heterogeneity, and responder/non-responder signatures from completed trial data
- Mine adverse event narratives, clinical notes, and investigator comments using NLP to surface latent safety signals
- Reconstruct patient-level longitudinal trajectories to model disease progression, drug response kinetics, and time-to-event outcomes
- Architect meta-analytic and cross-trial integrative workflows across completed studies
- Connect to large-scale biobank cohorts such as UK Biobank and All of Us for external validation and enrichment
- Establish reproducible research data management practices, including data versioning, containerized compute environments, and audit-ready analysis logs
- Ensure research activities comply with HIPAA, GDPR, and relevant IRB and ethics committee requirements
Requirements
What you’ll need- M.S. in Biomedical Informatics, Computational Biology, Bioinformatics, Statistical Genetics, Epidemiology, Computer Science or a closely related quantitative field or an MD/PhD with equivalent depth in translational data science, with 6+ years of research experience working with clinical trial datasets (SDTM/ADaM), biobank data, or large-scale population health data
- Or Ph.D. in Biomedical Informatics, Computational Biology, Bioinformatics, Statistical Genetics, Epidemiology, Computer Science or a closely related quantitative field or an MD/PhD with equivalent depth in translational data science, with 3+ years of research experience working with clinical trial datasets (SDTM/ADaM), biobank data, or large-scale population health data
- Demonstrated use of AI tools in production environments for clinical data analysis
- Expert proficiency in Python and/or R for statistical modelling and ML
- Strong command of SQL
- Experience with cloud-based research computing environments, ideally DNAnexus, AWS, GCP, Azure, or HPC clusters
- Familiarity with advanced generative AI methods such as LLM fine-tuning and building/training foundation models from scratch
- Experience with high-performance computing environments
- Deep knowledge of CDISC standards (SDTM, ADaM)
- Demonstrated experience applying survival analysis, causal inference, NLP, and deep learning to clinical or genomic research questions
- Thorough understanding of OMOP CDM, HL7 FHIR Genomics, and major biomedical ontologies
- Direct research experience with major public and restricted-access biobank resources such as UK Biobank and All of Us
- Experience with federated learning, differential privacy, or secure computation frameworks applied to multi-site biomedical research
- Track record of peer-reviewed publications in clinical AI, translational informatics, genomics, or a related field
- Familiarity with the target trial framework and its application in biobanks
- Knowledge of pharmacogenomics, drug response modeling, or PK/PD data analysis from clinical trials
- Experience with knowledge graph construction, graph ML, or ontology-driven reasoning for biomedical discovery
- Hands-on experience with multi-omic data analysis
- Must follow HIPAA, GDPR, and relevant IRB and ethics committee requirements
Benefits
Comp & perks- Company bonus depending, in part, on company and individual performance
- Company-sponsored 401(k)
- Pension
- Vacation benefits
- Medical benefits
- Dental benefits
- Vision benefits
- Prescription drug benefits
- Flexible benefits, including healthcare and/or dependent day care flexible spending accounts
- Life insurance and death benefits
- Time off and leave of absence benefits
- Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities
- Employee resource groups (ERGs)