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Clinical Research Study Coordinator Ocular Melanoma Research
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Full-time
- 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.
- The incumbent will complete data management, regulatory, and administrative tasks for an eye melanoma biorepository and associated repository research studies.
- Regulatory responsibilities include managing IRB submissions and maintaining required regulatory documents.
- Previous experience in clinical research setting desirable, preferably one year in a cancer research setting.
- High degree of computer literacy including word processing, statistical software (e.g., Stata, SAS, R), and database management programs (e.g. Study Trax and REDCap) helpful.
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