Clinical Research Coordinator - Emergency Medicine

The Ohio State University; Columbus (OH); On-site; USD 52,000 - 70,000; Full time

Job summary

The Ohio State University is seeking a Clinical Research Coordinator for Emergency Medicine in Columbus. You will coordinate daily clinical research activities, identify eligible patients, recruit and obtain informed consent, and ensure compliance with IRB, FDA, and sponsor regulations.

Responsibilities include coordinating schedules for procedures and testing, collecting data, assisting with data analysis, and contributing to protocol development and quality assurance activities.

Qualifications

• Bachelor’s degree in biological/health sciences or related field.
• At least 1 year of clinical research experience.

Responsibilities

• Coordinate and perform daily clinical research activities per approved protocols.
• Identify eligible patients and recruit/enroll with informed consent.
• Ensure compliance with IRB, FDA, and sponsor regulations.
• Collect, process and evaluate biological samples and data.
• Prepare reports and assist with external QA reviews.

Skills

Clinical research coordination

Regulatory compliance

Informed consent

Data collection

Education

Bachelor's degree in biological sciences/health sciences

Job description

Job Title: Clinical Research Coordinator - Emergency Medicine

Department: Medicine | Emergency Medicine

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.

The university is an equal opportunity employer, including veterans and disability.