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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