This work requires advanced skills in molecular and cellular biology, interpersonal communication, project management, professional research presentations, and reporting. The individual is responsible for identifying study subjects, gathering clinical data, obtaining informed consent according to the approved IRB protocol, and coordinating sample collection in collaboration with Kellogg Eye Center clinical staff. Tasks include preparing tissue samples for single-nucleus RNA-seq, data analysis, primary cell culture, 3-D organoid preparation, CRISPR-Cas9 library screening, and statistical data analysis. You must work closely with the PI and be responsible for reporting data at quarterly meetings with the sponsor.