CRAs have the responsibility for recruiting investigators, initiating studies, monitoring and closing down clinical sites at the end of studies. In addition, CRAs are expected to be able to write protocols, study design, design Clinical Report Forms and write Final Reports when studies are completed. Monitoring that the physician adheres to Good Clinical Practices and the study protocol; Performing study drug accountability; Verifying the documentation of the informed consent process for each study subject; Ensuring that non-serious and serious adverse experiences are properly documented and reported; Reviewing the case report form against the subject’s medical record for completeness and accuracy; Ensuring the filing and maintenance of the required regulatory documents.