Per Diem Clinical Research Coordinator-OB/GYN

The Per Diem Clinical Research Coordinator performs all the regular duties of a full or part time Clinical Research Coordinator, but on an as-needed basis. In addition, due to a limited number of hours, does not apply for Exempt status as is normal in this group. This individual assists in activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information, and may perform phlebotomy duties. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

• Collates and tabulates research data.             
• Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.            
• Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.          
• Assists in preparing grant applications, IRB/GCO for submission and filings.          
• Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.    
• May perform phlebotomy functions.   
• Secures, delivers and ships clinical specimens as required by the protocol.                         
• Prepares for monitoring visits.             
• Other assigned duties.

None but a health care background is a plus.