Clinical Research Coordinator - Anesthesiology

Overview Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Department of Anesthesiology; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, and other diagnostic testing in accordance with study protocol; participates in the collection, processing and evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, and provide appropriate level of care; documents unfavorable responses and notifies research sponsors and applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements. Responsibilities Coordinate and perform daily clinical research activities in accordance with approved protocols. Assess patient records to identify eligible participants for specified clinical research protocols. Recruit, interview and enroll patients; obtain informed consent and ensure consent process compliance with regulatory and sponsor requirements. Educate patients and families about the purpose, goals, and processes of the clinical study. Coordinate scheduling and follow-through of patient care appointments, procedures, and diagnostic testing per protocol. Participate in the collection, processing and evaluation of biological samples. Administer and evaluate standardized scoring of diagnostic, psychological or behavioral testing or questionnaires. Monitor patients for adverse reactions to study treatment, procedure or medication; notify appropriate clinical professional to evaluate patient response and complications. Document unfavorable responses and notify research sponsors and applicable regulatory agencies. Assess patient compliance related to the protocol. Assist with collecting, extracting, coding, and analyzing clinical research data; generate and review reports to ensure data validity. Support activities to ensure compliance with IRB, FDA, federal, state and industry sponsor regulations. Assist with coordinating and preparing for external quality assurance and control reviews by IRB and sponsors. Participate in developing new research protocols and contribute to 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. Required Experience One year experience in a clinical research capacity required. Experience And Skills Preferred Experience or knowledge in inpatient clinical research preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requirements and Other Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. CAREER/SUBFUNCTION: Research and Scholarship/Clinical Research CAREER BAND: Individual Contributor- Specialized

CAREER LEVEL: S2

This position is patient facing and is required to be onsite at The Ohio State University Wexner Medical Center. Evenings, weekends, holidays, and on-call hours may be required as dictated by the clinical research activity. Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact View email address on click.appcast.io. If you have questions while submitting an application, please review these frequently asked questions. Thank you for your interest in working at Ohio State. Equal Opportunity The university is an equal opportunity employer, including veterans and disability. #J-18808-Ljbffr The Ohio State University Wexner Medical Center