General DescriptionFaculty position available to study the molecular pathogenesis and CRISPR/Cas9 gene therapy of corneal diseases. The successful candidate will be highly motivated with a doctoral degree in a biomedical field and direct experience in molecular and cell biology, CRISPR/Cas9 gene editing, mammalian cell and ex vivo tissue culture/transfection/viral transduction, and immunohistochemistry.
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QualificationsAt least 4 years of post-doctoral experience is required. The role will involve continuation of an active research program investigating potential applications of CRISPR/Cas9 gene editing approaches for the treatment of corneal dystrophies as well as basic pathogenic mechanisms of the same disorders. Application InstructionsPlease submit your application, cover letter, and curriculum vitae via interfolio by clicking the "Apply Now" button. |
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