Clinical Research Coordinator-IRP OB/GYN Maternal Fetal Med

The Ohio State University; Columbus (OH); On-site; USD 42,000 - 58,000; Part time

Job summary

The Ohio State University is seeking a Clinical Research Coordinator for the Maternal Fetal Medicine division in the Department of Obstetrics and Gynecology. The role involves coordinating daily clinical research activities, recruiting patients, obtaining informed consent, and ensuring protocol compliance.

The position requires a Bachelor’s degree in biological or related fields and at least one year of clinical research experience, with preference for maternal fetal medicine knowledge and

Qualifications

• One year of clinical research experience preferred.
• Experience or knowledge in maternal fetal medicine is a plus.
• Computer skills with Microsoft Office applications desired.

Responsibilities

• Coordinate and perform daily clinical research activities according to approved protocols.
• Recruit, interview, enroll patients and obtain informed consent.
• Monitor patient safety and ensure regulatory compliance with IRB and FDA requirements.

Skills

Clinical research

Regulatory compliance

Education

Bachelor’s Degree in Biological sciences or related field

Tools

Microsoft Office

Job description

Job Title:Clinical Research Coordinator-IRP OB/GYN Maternal Fetal MedDepartment:Medicine | Obstetrics and Gynecology-JM

Job Summary: 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 Maternal Fetal Medicine Division in the Department of Obstetrics and Gynecology; 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, 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, & 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.

Skills and/or Experience Preferred: Experience or knowledge in maternal fetal medicine; 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.

FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research

CAREER BAND: Individual Contributor-Specialized

CAREER LEVEL: S2

Additional Information:Location:McCampbell Hall (0303)Position Type:IntermittentScheduled Hours:0.2Shift: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.

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