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Senior Scientist - PKDM (NAMs-Based Translational ADME Sciences)

Amgen
Full-time
Remote friendly (South San Francisco, CA)
United States
Clinical Research and Development

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Role Summary

Senior Scientist - PKDM (NAMs-Based Translational ADME Sciences)

Responsibilities

  • Lead the development and qualification of high-fidelity, human-relevant in vitro models, including 3D cultures and microphysiological systems, to assess drug disposition, biotransformation, and pharmacodynamic effects.
  • Design and execute experimental strategies that integrate quantitative endpoints, enabling correlation of exposure and response across NAMs and traditional models.
  • Advance throughput and data scalability by implementing assay miniaturization, plate-based automation, and high-content imaging workflows.
  • Apply deep cell biology expertise to refine parenchymal–stromal co-culture systems and incorporate complementary analytical endpoints to define cellular phenotype and pharmacodynamic response.
  • Characterize responses using flow cytometry, multiplexed analytical sampling, confocal microscopy, and live-cell imaging (e.g., Incucyte).
  • Adopt computational tools and quantitative data pipelines to streamline analysis of complex kinetic and imaging datasets.
  • Collaborate across disciplines to define mechanism-based PK liabilities, support dose selection hypotheses, and guide preclinical-to-clinical translation.
  • Communicate findings clearly and effectively to inform cross-functional teams and drive data-driven decision-making in a fast-paced R&D environment.

Qualifications

  • Basic Qualifications: Doctorate degree in Biomedical Engineering, Pharmacology, Systems Biology, Cellular & Molecular Biology, Biophysics, or a related discipline (and relevant post-doc where applicable); or Master’s degree and 3 years of relevant industry experience; or Bachelor’s degree and 5 years of relevant industry experience.
  • Preferred Qualifications:
    • 2+ years of postdoctoral or industry experience applying 3D cellular or microphysiological systems to study drug disposition or disease biology.
    • Demonstrated experience in cell model and/or MPS device fabrication, culture, and integration with analytical readouts.
    • Working understanding of pharmacokinetic principles for small and large molecules and of preclinical ADME processes (absorption, distribution, metabolism, and excretion).
    • Familiarity with bioanalytical and imaging techniques supporting quantitative in vitro pharmacology.
    • Strong communication, data interpretation, and collaboration skills; ability to synthesize complex data into actionable insights for multidisciplinary project teams.
    • Demonstrated ability to innovate, adapt, and deliver in a dynamic research environment.

Skills

  • 3D organoid and microphysiological system platforms
  • In vitro pharmacology assays, flow cytometry, imaging, and data analysis
  • Quantitative data integration across NAMs and traditional models
  • Co-culture system design and biomarker endpoints
  • Computational data pipelines and statistical interpretation
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