Clinical Research Assistant - CCC Total Cancer Care Program

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Position Summary

Clinical Research Assistant who provides daily operational support to the Total Cancer Care Program, TCCP, in the Comprehensive Cancer Center; serves as a liaison to administration for issues pertaining to gathering patient informed consent for biospecimen research; obtains patient informed consents at the James Cancer Hospital, University Hospital and clinics; coordinates work activities with team members; assists in the design of new consenting methods and data processing systems to maintain patient confidentiality; collects, maintains and analyzes patient research data; prepares reports; maintains supplies and coordinates quality control processes; manages documentation related to patients on clinical trials; assists with preparation of meeting materials.

Job Requirements

Bachelor's degree in biological sciences, health sciences, social sciences, psychology, human ecology or other medical field or an equivalent combination of education & experience required.

Experience in a clinical research capacity or setting desired; experience with collection, analysis and management of clinical research data strongly desired; certification in a clinical research professional society desired; human subjects training and experience in a clinical and/or research setting working with patients desired; computer skills required with experience utilizing Microsoft software applications desired; considerable experience utilizing database applications desired.

Research and Scholarship - Clinical Research - Individual Contributor - Technical - T2

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

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