Clinical Research Coordinator - Emergency Medicine

Ohio State University; Columbus (OH); Hybrid; USD 52,000 - 72,000; Full time

Job summary

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols within the Department of Emergency Medicine.

The role includes assessing patient records for eligibility, recruiting and enrolling participants, obtaining informed consent, and educating patients and families about the study. It also involves scheduling, data collection, and ensuring regulatory compliance.

Qualifications

• Bachelor’s degree required in biological/health/social sciences or related field.
• One year of experience in a clinical research capacity required.

Responsibilities

• Coordinate and perform daily clinical research activities per approved protocols.
• Assess patient records to identify eligibility and enroll participants.
• Obtain informed consent and educate patients and families about study purpose and process.
• Coordinate scheduling and follow‑through of appointments, procedures and testing.
• Assist with data collection, processing and analysis to ensure data integrity.

Education

Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required

Job description

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Department of Emergency Medicine 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, & other diagnostic testing in accordance with study protocol; participates in the collection, processing & evaluation of biological samples; administers 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, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & 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. **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. ## Additional Information:## Location:Prior Hall (0302)## Position Type:Regular## Scheduled Hours:40## **Shift:**Varying Shifts***Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.***