Clinical Research Assistant

Job Description

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.

Minimum Education Required

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

Qualifications

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