Clinical Research Coordinator - Radiology

Ohio State University; United States; On-site; USD 52,000 - 78,000; Full time

Job summary

Ohio State University seeks a Clinical Research Coordinator in Radiology to coordinate daily clinical research activities, screen and recruit participants, obtain informed consent, and ensure protocol compliance.

You will manage scheduling, data collection, sample handling, adverse event monitoring, and regulatory documentation, supporting IRB/FDA compliance and sponsor reporting.

Qualifications

• Bachelor’s degree in biological or health sciences required.
• Minimum one year of clinical research experience.
• Imaging methodologies knowledge or experience preferred.
• Microsoft Office proficiency required.
• Background check and pre-employment screening may be required.

Responsibilities

• Coordinate daily clinical research activities per approved protocols.
• Screen, recruit, and enroll eligible participants.
• Obtain informed consent and ensure regulatory compliance.
• Collect, process, and manage data and specimens.
• Monitor safety and report adverse events to appropriate staff.

Skills

Clinical research

IRB compliance

Participant recruitment

Data collection

Education

Bachelor's degree

Clinical research certification (desired)

Tools

Microsoft Office

Job description

Job Title

Clinical Research Coordinator - Radiology

Department

Medicine | Radiology

Job Description Summary

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Center for Clinical Research Management in the Department of Radiology; 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, evaluates and calculates standardized scoring of diagnostic 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, & 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 and Skills/Experience Required/Desired

Bachelor's Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity required; experience or knowledge in imaging methodologies 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. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.

Additional Information

Location: Twelfth Ave, 395 W (0356)

Position Type: Regular

Scheduled Hours: 40

Shift: First Shift

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.