Research Services Clinical Sciences Professional, Intermediate to Senior

Key Responsibilities

• Aid in and oversee the daily operations of clinical trials and studies.
• Obtain study subject's medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subjects to participate in clinical trials.
• Perform informed consent processes or ensure that the informed consent process has occurred, is properly documented, and that informed consent forms are filed as required.
• Interview prospective subjects for various research clinical trials, educate potential subjects on the details of the studies through phone contacts and personal interviews.
• Schedule subject participation in research clinical trials, coordinating availability of necessary space and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
• Collect, code, and analyze 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 subject recruitment efforts, including communicating with patients expressing an interest and conducting all pre-screening/screening activities.
• Ensure that the necessary supplies and equipment for studies are in stock and in working order.

Qualifications

• Bachelor’s degree in biology, molecular biology, chemistry, genetics, or a related field.
• A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year-for-year basis.