The Tisch Cancer Center brings together a vast range of renowned specialists and resources for cancer care, and provides access to exceptional medical care for other conditions, as needed.

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.

• Bachelor’s in Science or closely related field or equivalent experience
• None but a health care background is a plus

Please pay attention to fraud and not pay any money to any person or entity that is not trusted, inspect the commodity and ensure its safety before completing the deal, and report violating advertisements immediately..