Responsibilities Include:

• Reviewing patient records to determine patient eligibility for participating in research protocol. 
• Analyzing appropriate data for recruitment purposes and interview patients for protocol to determine patient commitment.  
• Responsible for completing all data entry requirements accurately including data entry of patient registration; entry of test order from requisition or pulling order from database; managing Standing Orders.  
• Collecting, organizing, cataloging, disseminating, and maintaining appropriate files of current patient data.  
• Assisting with monitoring audits/visits for clinical protocols. 
• Processing specimens, including labeling, centrifuging, splitting, and freezing specimens as required by test order. 
• Performing clerical duties when assigned such as data entry, inventory, stock supplies, and answer phones when needed. 
• Maintaining all appropriate phlebotomy logs in a timely manner and based on frequency, such as maintenance logs and temperature logs.  
• Completing training courses and keeping up to date with the certifications.  
• Assisting with regulatory, research or administrative compliance.  
• Assisting with preparation and delivery of required reports and other research documentation.   
• Having strong written and oral communication, interpersonal skills and attention to detail.  
• Working under minimal supervision and being goal oriented.