Protocol Development and Recruiting

• The CRC draws up a step-by-step plan for the clinical trial and recruits subjects relevant to the focus of the study. This includes drafting and executing an informed consent document.
  
  

Tests and Procedures Scheduling

• Organized scheduling of subject visits for testing and following protocol are crucial to a successful trial. The CRC must ensure that subject activity is done appropriately with meticulous record keeping for research and legal purposes.
  
  

Data Collecting and Budget Managing

• The CRC collects all pertinent trial data and maintains an accurate database that can be used for investigative study. In addition, the CRC can be held accountable for budget spending and grant procurement.