Northern California HERC

Clinical Research Assistant to provide daily operational support to Total Cancer Care, TCC, 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; ensures actions are taken directly or indirectly to eliminate causes of protocol violation; ensures that all federal and local quality guidelines, including Good Clinical Practice (GCP), are followed; attends study meetings; provides weekly updates and progress reports on study activities including recruitment and follow-up activities; other administrative duties as needed.

Minimum Required Qualifications

Bachelors Degree in biological sciences or biology or an equivalent combination of education and experience required. Highly organized with attention to detail; excellent verbal and written communication skills. Microsoft (MS) Office products and REDCap experience desirable.

Function: Research and Scholarship
Subfunction: Clinical Research
Career Band: Individual Contributor - Technical
Career Level: T2

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