Sr Scientist/Principal Scientist - Genomics Sciences
Listed on 2026-07-02
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Research/Development
Biotech Research, Research Scientist
The Genomic Sciences team within Lilly Genetic Medicine/RNA Therapeutics is seeking a senior experimental genomics expert to lead and execute genomics assays in support of the discovery and development of RNA medicines. This role is embedded in a high-throughput genomics screening environment that generates decisional data for siRNA and antisense oligonucleotide programs across the LGM portfolio. The successful candidate will be a hands‑on experimentalist with strong technical skills in next-generation sequencing (NGS), a commitment to rigorous sample management and documentation, and a desire to contribute meaningfully to the advancement of genetic medicines.
Key Responsibilities- Execute and optimize NGS library preparation workflows (e.g., 3’ RNA‑seq, mRNA‑seq) across targeted and large-scale screening campaigns, maintaining high quality and throughput
- Track, document, and QC samples through all stages of assay development
- Develop, troubleshoot, and refine genomics assay protocols to meet evolving program needs, including new library chemistries, multiplexing strategies, and sample input optimization
- Maintain impeccable sample tracking, chain‑of‑custody documentation, and electronic lab notebook records in compliance with Lilly quality standards
- Collaborate closely with computational genomics, medicinal chemistry, and biology colleagues to ensure experimental designs generate robust, interpretable, and decisional data
- Participate actively in cross‑functional project teams, contributing scientific perspective on assay design, data interpretation, and experimental prioritization
- Support lab infrastructure including reagent inventory, equipment maintenance, and continuous improvement of standard operating procedures
- Bachelor’s degree in genomics, molecular biology, biochemistry, genetics, or a related discipline with a minimum of 3+ years of relevant laboratory experience; or Master’s degree in genomics, molecular biology, biochemistry, genetics, or a related discipline with a minimum of 1+ years of relevant laboratory experience
- Qualified applicants must be authorized to work in the United States on a full‑time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F‑1 CPT, F‑1 OPT, F‑1 STEM OPT, J‑1, H‑1B, TN, O‑1, E‑3, H‑1B1, or L‑1
- Demonstrated hands‑on experience with NGS library preparation, quality control (Qubit, Tape Station/Bioanalyzer, qPCR‑based quantification), and sequencer operation
- Strong organizational skills with meticulous attention to sample management, documentation, and experimental reproducibility
- Ability to work effectively in a fast‑paced, team‑oriented research environment generating high‑quality decisional data at scale
- Experience with high‑throughput or pooled screening workflows in a pharmaceutical or genomics core environment
- Experience with single cell genomics or spatial transcriptomics data
- Familiarity with RNA therapeutics biology (siRNA, ASO) and associated transcriptomic readouts
- Bioinformatics experience including comfort with command‑line tools, scripting (R, Python), and/or analysis of NGS data (alignment, QC metrics, differential expression)
- Experience with automation platforms (e.g., Hamilton, Beckman) for library preparation or sample handling
- Track record of method development or assay optimization in a research or development setting
- Experience using and developing ELN based documentation tools
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.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $71,250 - $187,000. Full‑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.
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