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Sr. Principal Scientist

Job in Clifton, Passaic County, New Jersey, 07015, USA
Listing for: Legend Biotech USA
Full Time position
Listed on 2026-08-08
Job specializations:
  • Research/Development
    Research Scientist, Data Scientist, Biotech Research, Immunology Research
Salary/Wage Range or Industry Benchmark: 150000 - 190000 USD Yearly USD 150000.00 190000.00 YEAR
Job Description & How to Apply Below

Legend Biotech is seeking a Sr. Principal/Principal Scientist as part of the Research & Early Development team based in Somerset, NJ
.

Role Overview

Legend Biotech is seeking a highly experienced Senior Principal Scientist / Principal Scientist - Flow Cytometry to provide scientific leadership and hands-on expertise in flow cytometry to support cell and gene therapy programs from IND-enabling studies through early-and late-stage clinical development. This role is critical for ensuring scientific rigor, data quality, and strategic insight across in-house and outsourced flow cytometry activities, including assay development, validation, CRO oversight, and deep data interpretation to support translational, PK/PD, and regulatory decision-making.

Key Responsibilities
  • Lead the design, development, optimization, qualification, and validation of multicolor and spectral flow cytometry assays supporting IND-enabling animal studies and clinical trials.
  • Provide subject-matter expertise in panel design, antibody and reagent qualification, gating strategies, and data analysis for complex immunophenotyping applications.
  • Conduct deep scientific review and interpretation of flow cytometry datasets to support PK/PD, mechanism-of-action, and translational insights.
  • Serve as the primary scientific lead for external laboratories and CROs performing flow cytometry assays.
  • Oversee assay transfer, validation, execution, troubleshooting, and data delivery at CROs.
  • Ensure outsourced activities meet Legend quality standards, regulatory expectations, and program timelines.
  • Identify risks related to assay performance, data quality, and operational execution, and implement mitigation strategies.
  • Author, review, and approve bioanalytical assay validation reports, study reports, and regulatory documentation.
  • Ensure flow cytometry assays and data packages are inspection-ready and compliant with GxP principles and data integrity requirements.
  • Contribute to bioanalytical sections of IND and other regulatory submissions.
  • Partner with Clinical, Translational Research, Biomarkers, Nonclinical Safety, and Data Science teams to align assay strategy with program objectives.
  • Provide scientific input to study design, endpoint selection, and interpretation of bioanalytical results.
  • Communicate complex data clearly to multidisciplinary stakeholders.
  • Establish and maintain SOPs, best practices, and governance for in-house flow cytometry workflows.
  • Mentor and scientifically guide junior scientists and associates.
  • Evaluate and implement new technologies, platforms, and analytical approaches to enhance capabilities.
Requirements
  • Ph.D. in Immunology, Cell Biology, Molecular Biology, or related discipline with 8+ years (Principal Scientist) or 10+ years (Senior Principal Scientist) of relevant industry experience; or M.S. with 12+ years of experience.
  • Extensive hands-on experience with multicolor and spectral flow cytometry platforms.
  • Demonstrated experience supporting cell therapy and/or gene therapy programs.
  • Strong understanding of bioanalytical method development, validation, and regulatory expectations.
  • Proven ability to lead complex programs, influence cross-functional teams, and provide strategic scientific direction.
  • Experience overseeing CROs and external vendors.
  • Excellent written and verbal communication skills.
  • Experience with CAR-T, in vivo gene delivery, or other advanced cell therapy platforms.
  • Experience contributing to IND-enabling or regulatory filings.
  • Background in translational PK/PD applications of flow cytometry.

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.

Please note:
These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

Work Authorization & Employment Eligibility

Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your…

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