Clinical Research Coordinator – IRP OB/GYN, Maternal Fetal Medicine

The Ohio State University, Main Campus

. Coordinate and perform daily clinical research activities in accordance with approved protocols for the Maternal Fetal Medicine Division .

Posted 10/14/2026part-timeOhio • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating clinical research activities, including patient recruitment, informed consent, and data analysis, while ensuring compliance with regulatory standards. Proficient in managing patient care and evaluating clinical research protocols in the Maternal Fetal Medicine domain.

Highest-signal resume keywords

Clinical Research CoordinationPatient Recruitment and EnrollmentInformed Consent ComplianceData Collection and AnalysisMaternal Fetal Medicine Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData AnalysisBiological Sample ProcessingStandardized Testing AdministrationPatient MonitoringProtocol Compliance EvaluationReport GenerationMedical Terminology KnowledgeClinical Research Data CodingQuality Assurance Support

Soft Skills

Patient EducationCommunication SkillsInterpersonal Skills

Tools & Technologies

Microsoft Software Applications

Certifications & Qualifications

Clinical Research Certification

Industry Keywords

Maternal Fetal MedicineIRB ComplianceFDA RegulationsClinical Research ProtocolsRegulatory Agency Notification

About the role

Key responsibilities & impact

Coordinate and perform daily clinical research activities in accordance with approved protocols for the Maternal Fetal Medicine Division
Assess patient records to identify eligible clinical research participants
Recruit, interview, and enroll patients
Obtain informed consent in compliance with regulatory and sponsor requirements
Educate patients and families about clinical study purposes, goals, and processes
Coordinate patient care appointments, procedures, and diagnostic testing according to study protocols
Collect, process, and evaluate biological samples
Administer, evaluate, and calculate standardized diagnostic, psychological, or behavioral testing and questionnaires
Monitor patients for adverse reactions and notify appropriate clinical professionals
Document unfavorable responses and notify research sponsors and regulatory agencies
Evaluate patient protocol compliance
Collect, extract, code, and analyze clinical research data
Generate reports and review data validity
Support compliance with IRB, FDA, federal, state, and industry sponsor regulations
Assist with external quality assurance and control reviews
Participate in developing new research protocols and establishing study goals

Requirements

What you’ll need

Bachelor’s Degree in biological sciences, health sciences, social sciences or another medical field, or an equivalent combination of education and experience
One year of experience in a clinical research capacity
Computer skills required
Successful completion of a background check
Varying shifts
Experience or knowledge in maternal fetal medicine preferred
Knowledge of medical terminology desired
Clinical research certification from an accredited certifying agency desired
Experience using Microsoft software applications desired

Benefits

Comp & perks

Equal opportunity employer, including veterans and disability
Potential pre-employment physical and drug screen as part of the post-offer process