Scheduled Hours40Position SummaryJoin a vibrant research team focused on discovering the genomic, genetic, cellular and molecular determinants that cause nervous system dysfunction in people with a common neurogenetic disorder, Neurofibromatosis type 1 (NF1). Children with NF1 are at risk for brain and nerve tumors, vision loss, learning problems, autism, and developmental disabilities. This position assists with the technical aspects of studies and experiments, including documentation and preparation of materials. Those interested in a research or medical career in neuroscience, neurology, ophthalmology, or genetics are encouraged to apply.
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