{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/indiana/"},"x-facet":{"type":"city","slug":"indiana","display":"Indiana","count":3},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. 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Ensure that complex datasets are accurate, consistent, traceable, and translated into actionable insights that support compound profiling, lead optimization, and data-driven program decisions.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Manage and curate LC/MS datasets from non-regulatory ADME bioanalysis studies supporting exploratory and pilot toxicology in vivo PK/PD studies</li>\n<li>Ensure the accuracy, completeness, consistency, and traceability of data from raw LC/MS outputs through processed results and internal reports</li>\n<li>Perform scientific quality-control reviews to identify outliers, errors, and analytical or method-related artifacts</li>\n<li>Evaluate ADME parameters across compounds, projects, and assay formats to support structure-activity and structure-property relationships</li>\n<li>Collaborate with DMPK, analytical, informatics, and project teams to interpret data and improve pipelines, automation, visualization tools, and analytical efficiency</li>\n<li>Coordinate internal and external CRO data contributions while maintaining alignment among study designs, metadata, analytical methods, and final outputs</li>\n<li>Prepare clear summaries, tables, figures, dashboards, and integrated discovery data packages to support compound progression and portfolio decisions</li>\n<li>Establish standardized data formats, naming conventions, metadata practices, and reproducible workflows for downstream analysis and knowledge sharing</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor’s or master’s degree in analytical chemistry, pharmacokinetics, pharmaceutical sciences, biochemistry, or a related scientific field</li>\n<li>3–7+ years of experience working with LC/MS data in discovery stage ADME or DMPK settings</li>\n<li>Strong understanding of LC/MS workflows, quantitative data analysis, and common discovery ADME assays</li>\n<li>Experience evaluating data quality and identifying analytical, method-related, and data-processing artifacts</li>\n<li>Familiarity with high-resolution mass spectrometry bioanalytical data and workflows for large molecules, new drug modalities, or biomarkers</li>\n</ul>\n<p><strong>The Knowledge, Skills and Abilities Needed for This Role</strong></p>\n<ul>\n<li>Strong analytical thinking and the ability to translate complex scientific datasets into clear, actionable insights</li>\n<li>Scientific rigor, attention to detail, and a strong data-integrity mindset when managing complex datasets</li>\n<li>Effective cross-functional collaboration with bioanalytical scientists, DMPK teams, project coordinators, study directors, CROs, informatics teams, and IT partners</li>\n<li>Ability to communicate data assumptions, limitations, trends, inconsistencies, and conclusions clearly to scientific stakeholders</li>\n<li>Strong organizational skills and the ability to establish standardized, reproducible data-management practices</li>\n<li>Knowledge of bioanalytical workflows for modalities such as oligonucleotides, proteins, peptides, antibody-drug conjugates, ionizable lipids in lipid nanoparticles, and amino acids</li>\n</ul>\n<p><strong>What We Offer You</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. 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You will collaborate with clients and cross-functional teams to deliver scientifically rigorous solutions supporting drug development programs.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Serve as Primary Investigator on scientific client studies, conducting laboratory work and communicating progress and results</li>\n<li>Design and execute complex method development experiments for large-molecule therapeutic candidates</li>\n<li>Evaluate and implement new bioanalytical methods, technologies, and instrumentation for client programs</li>\n<li>Prepare technical summary reports, proposals, and protocols, including reports that may support FDA submissions</li>\n<li>Provide meaningful data analysis and interpretation, including statistical analysis of experimental findings</li>\n<li>Manage multiple complex technical projects and guide or mentor junior scientific staff</li>\n<li>Collaborate across functions to deliver client studies and deploy methods across multiple programs</li>\n<li>Maintain laboratory notebooks, equipment standards, and compliance with applicable SOPs, regulatory requirements, and good documentation practices</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Ph.D. in Chemistry, Analytical Chemistry, Biochemistry, Chemical Biology, Biology, or a related field preferred; 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