Principal Scientist - Translational Medicine, Oncology

Roche•South San Francisco, CA
•$141,500 - $262,900•Hybrid

About The Position

As a Principal Scientist in Translational Medicine Oncology, you will serve as a vital scientific anchor bridging discovery research and clinical development. You will lead biomarker discovery and translational strategy for innovative oncology clinical pipelines, working directly on early- to late-stage clinical programs.

Requirements

  • Hold a PhD, MD, or MD/PhD in Molecular Biology, Cancer Biology, Immunology, Computational Biology, Bioinformatics, or a related life sciences discipline.
  • Possess significant graduate or postdoctoral research experience demonstrating scientific excellence and rigor through a record of first-author publications in peer-reviewed journals.
  • Prior post-graduate industry experience or significant postdoctoral experience is required.
  • Bring hands-on experience or deep technical fluency in translational research methodologies, including molecular profiling, multi-omics, single-cell genomics, spatial biology, or functional immune assays.
  • Exhibit exceptional cross-functional collaboration and communication skills, with a proven ability to translate complex biological concepts into actionable clinical insights across multidisciplinary teams.

Nice To Haves

  • Prior industry experience within oncology drug discovery, translational oncology, or clinical development.
  • Deep subject matter expertise or focused research background in oncogenic signaling, RAS biology, non-small cell lung cancer (NSCLC), or colorectal cancer (CRC).
  • Demonstrate proficiency with or solid exposure to computational biology workflows and biological data analysis (familiarity with R and/or Python).
  • Practical experience or strong enthusiasm for leveraging machine learning and emerging agentic/generative AI tools to accelerate translational discovery and multi-modal data interpretation.
  • Experience collaborating on companion diagnostics (CDx) development and clinical protocol execution.

Responsibilities

  • Design, implement, and drive end-to-end pharmacodynamic and predictive biomarker strategies across first-in-human through registrational clinical studies.
  • Champion hypothesis-driven translational research to identify novel biomarkers of therapeutic response, mechanisms of clinical resistance, and tumor microenvironment dynamics.
  • Integrate and leverage high-dimensional data—including multi-omic profiling, spatial biology, single-cell platforms, and functional immune assays—in partnership with computational scientists and AI-driven platforms.
  • Lead the authoring, review, and strategic integration of biomarker and translational sections within clinical trial protocols, regulatory submissions, clinical study reports, and investigator brochures.
  • Partner cross-functionally across Research, Clinical Development, Clinical Pharmacology, Companion Diagnostics, Biostatistics, and Clinical Operations to ensure seamless scientific alignment.
  • Partner with Operations team to provide scientific leadership and strategic guidance for trial design, implementation, and conduct.
  • Drive scientific engagement externally with academic collaborators, clinical trial investigators, and key opinion leaders (KOLs) while disseminating breakthrough science via high-impact peer-reviewed publications and conference presentations.

Benefits

  • A discretionary annual bonus may be available based on individual and Company performance.
  • This position also qualifies for the benefits detailed at the link provided below.

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What This Job Offers

Job Type

Full-time

Career Level

Principal

Education Level

Ph.D. or professional degree

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