Job Description

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Job Title

Clinical Research Assistant

Department

CCC | Clinical Trials Office

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

Bachelor’s 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.

Additional Information

Location:

Gateway C (0863)

Position Type

Regular

Scheduled Hours

40

Shift

First Shift

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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Applicants are encouraged to complete and submit the Equal Employment Identification form.

Job Tags

Full time, Shift work, Day shift,

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