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Clinical Research Associate - Oncology Research - Full Time SUMMARY: Accountable for assisting investigators in screening patients for potential study enrollment, assists in the scheduling of patients for study visits as per the study protocol, creating study documents, extrapolating data and completing electronic data submissions. Prepares for and participates in monitoring and auditing activities. Responsible for processing, filing and maintaining protocol regulatory documents. Coordinates in the collection and shipment of specimens, imaging documents and other items per the study protocol. Collaborates and participates in identifying and addressing quality assurance issues and developing departmental standards. Assures compliance with the IRB (Local or CIRB