Job Description:

Supports clinical research projects by facilitating finalization on medical research protocols, managing final approvals of procedures, and assisting research faculty with future trials by study protocol drug and device advisement. Prepares, writes, and presents updated protocols. Works directly with patients and takes medical histories, performs exams, obtains biological specimens, assists with procedures, schedules tests, and performs study-specific protocols. Acts as liaison to regulatory bodies and reports to auditing bodies. Ensures regulatory adherence.