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therapy, with a particular emphasis on epigenetic regulation, radiation response, and treatment resistance. Our work leverages patient-derived organoids, engineered cellular models, functional genomics, and
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cancer models and patient-centered translational approaches to define mechanisms that regulate treatment response, immune evasion, and disease progression. Candidates with experience in cancer biology
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proteostasis, cytoskeletal dynamics, and ferroptotic cell death. This collaborative work combines biochemistry, chemical biology, cell signaling, live-cell imaging, and organotypic brain slice models to dissect
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and anticipated conferral date. Experience working with rodent models of pain, inflammation, neuroscience, or related biomedical research. Demonstrated ability to independently design, execute, analyze
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and supporting a collegial and inclusive team culture. For more about our laboratory, visit: https://sites.duke.edu/franzlab/ Appointment details: • Start date: October 2026 (flexible) • Duration
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R or Python programming Tissue culture techniques Animal models Interest in translational cancer research, immunotherapy, and neuro-oncology. Other Requirements Ability to work with patient-derived
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, and other relevant cell types. Conduct stereotaxic surgical procedures and targeted injections in mouse models. Support viral vector delivery and molecular, biochemical, histological, and cellular
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, and apply Crainbow mouse models that express multiple HER2 isoforms — wild-type (WT), D16, and p95 which are essential reagents for the laboratory’s DoD funded program. Minimum Requirements: Ph.D
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, epigenomics, single-cell technologies, stem cell biology, muscle biology, aging, immunology, gene and cell therapy, computational analysis, or animal models are especially encouraged to apply. Strong motivation
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in AI for genomics (e.g., generative models, transformers, genomic language models, agentic AI) and related areas of statistics (e.g., uncertainty quantification for machine learning and AI). Apply