This position is responsible for assessing the clinical significance of genomic variants, identified in patient samples. Duties include literature curation, interpreting sequence variants in the context of cancer
biology/heritable disorders, and generating reports which summarize genomic data in the context of clinical care. The majority of time is spent analyzing clinical cases with special projects for process improvement. This position demands high caliber, attentive
to detail, and focused individuals. This is a dynamic position that requires the ability to work independently as well as in a team environment.
Physical and other requirements: