Principal Bioinformatician

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life‑threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T‑cell, T‑cell receptor (TCR‑T), and natural killer (NK) cell‑based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting‑edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta‑cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Principal Bioinformatician as part of the Early Drug Development team based in Somerset, NJ or Remotely . Role Overview This role is to support translational strategies across pipeline development programs. He/She will lead computational analyses integrating multi‑modality clinical, and biomarker datasets to enable mechanism‑of‑action understanding, patient stratification, pharmacodynamic assessment, and support translational decision‑making. Key Responsibilities Translational Biomarker Analysis with multi‑modality and multi‑omics assays such as Bulk and Single cell RNA‑seq, TCR/BCR‑seq, WGS/WES, Amplicon‑seq, ATAC‑seq, ctDNA/liquid biopsy, Proteomics and cytokine profiling, spatial and multiplex imaging, Flow cytometry/CyTOF. Support translational biomarker discovery and validation including identification of pharmacodynamic (PD), predictive, prognostic, and response biomarkers; integrated analyses correlating biomarker data with clinical outcomes, PK/PD measurements, safety for patient stratification and mechanism‑of‑action hypotheses. Build and maintain reproducible and scalable bioinformatics pipelines using cloud or high‑performance computing environments. Contribute to translational data infrastructure and data governance strategies. Ensure analysis reproducibility, traceability, and documentation compliance. Partner closely with translational scientists, clinical development, research and CMC teams, CROs and collaborators to help translate complex computational findings into biologically meaningful insights. Contribute to regulatory documentation required biomarker sections of INDs, IBs, clinical study reports and regulatory briefing documents. He/she has the authority to make decisions related to methodologies and approaches development processes, project execution timelines, milestones and resource allocation within budget. Higher‑level approvals are required for significant technical selection, budget allocations, strategic shifts, or major collaborations that have substantial scientific, financial or long‑term implications. Requirements PhD (5+ years) or MS (8+ years) in Bioinformatics, Computational Biology, Genomics, Systems Biology and related quantitative biological sciences. Strong expertise in bioinformatics, statistics with some biological training background, with experience in translational research in oncology, immunology or autoimmune disease. Gene and cell therapy involvement is a plus. Strong experience with R and/or Python programming, Linux/Unix computing environments, workflow management systems (e.g., Snakemake, Nextflow, WDL) with Cloud platforms (AWS, GCP, Azure) preferred. Pay and Benefits Pay Range (Base Pay): $146,410—$192,164 USD. Other types of pay: Performance‑based bonus and/or equity is available to employees in eligible roles. Benefits and paid time off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. Eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short‑ and long‑term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well‑being initiatives, and peer‑to‑peer recognition programs. Please note: These benefits are offered exclusively to permanent full‑time employees. Contractors are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. #J-18808-Ljbffr Merck & Co.