Description
Under the supervision of the Program Director, and in collaboration with Principal Investigators, the Clinical Research Coordinator contributes to clinical research studies in the Ocular Melanoma Center. This is a role that includes working with data and patients. The incumbent will complete data management, regulatory, and administrative tasks for an eye melanoma biorepository and associated repository research studies. Key responsibilities include generating and maintaining integrity of data, creating and managing study databases, and performing data analyses. Regulatory responsibilities include managing IRB submissions and maintaining required regulatory documents. This position will also involve providing back-up support to enroll study subjects and process blood and tumor specimens.
This role is Full Time M-F, 8:30-5.
Qualifications
Qualifications
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