Assist with and oversee the day-to-day operations of clinical trials and studies
Obtain study participant’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial
Perform informed consent processes and/or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required
Interview prospective participants for a variety of research clinical trials. Educate potential participants on the details of the studies through phone contacts and personal interviews
Schedule study participants in clinical trials, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)
Collect, code, and review data obtained from research in an accurate and timely manner
Adhere to research regulatory standards
Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
Participate in participant recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities
Participate in weekly research update meetings by preparing and updating study tracking documents
Ensure that the necessary supplies and equipment for studies are in stock and in working order
