*Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
*Code, evaluate, or interpret collected study data. Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
*Maintain required records of study activity including case report forms or regulatory forms.
*Participate in continuing education activities, or attend conferences and seminars to maintain current
knowledge of clinical studies affairs and issues.
*Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or
specially designated review groups. Perform specific protocol procedures such as interviewing subjects.