Clinical Research Assistant

Clinical Research Assistant to provide daily operational support to the Recruitment, Intervention, and Survey Shared Resource (RISSR), in the Comprehensive Cancer Center.

Responsibilities

• Serves as a liaison to administration for issues pertaining to gathering patient informed consent for biospecimen and/or human subjects 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 and prepares reports

• Maintains supplies and coordinates quality control processes; manages documentation related to patients on clinical trials

• Assists with preparation of meeting materials

Minimum Required Qualifications

Bachelors Degree in biological sciences, health sciences or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity experience or knowledge in clinical research required; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired.