Clinical Research Coordinator Float-Clinical Trials Management Office

Job Title: Clinical Research Coordinator Float Department: Medicine | Clinical Trials Management Office Responsibilities Coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non‑oncology human subjects research; assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruit, interview and enroll patients; obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements; educate patients and families of purpose, goals, and processes of clinical study; coordinate scheduling and follow‑through of patient care appointments, procedures, and other diagnostic testing in accordance with study protocol; participate in the collection, processing, and evaluation of biological samples; administer, evaluate and calculate standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assist with monitoring patients for adverse reactions to study treatment, procedure or medication, notify appropriate clinical professional to evaluate patient response, identify status of complications and provide appropriate level of care; document unfavorable responses and notify research sponsors and applicable regulatory agencies; participate in evaluating patients for compliance related to protocol; assist with collecting, extracting, coding, and analyzing clinical research data; generate reports and reviews to ensure validity of data; support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participate in activities to develop new research protocols and contribute to establishment of study goals to meet protocol requirements. Minimum Education Required Bachelor’s Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required. Minimum Experience Required One year experience in a clinical research capacity required. Computer experience required. Experience Preferred Experience or knowledge in coordinating clinical trials preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired. Experience using Microsoft applications desired and knowledge of database systems such as RedCap, Medidata, Rave, etc. Background & Physical Requirements Requires successful completion of a background check. Qualified candidates may be requested to complete a pre‑employment physical, including a drug screen. Position Details This position is patient facing and is required to be on site. Travel to various clinical research locations will be required. Locations may include Outpatient Care East, Outpatient Care New Albany, Outpatient Care Dublin, Martha Morehouse, Upper Arlington, etc. Location: Dodd Hall (0171). Position Type: Regular. Scheduled Hours: 40. Shift: First Shift. University is an equal opportunity employer, including veterans and disability. #J-18808-Ljbffr The Ohio State University