FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Clinical Research Coordinator – Radiology
The Ohio State University, Main Campus. Coordinate and perform daily clinical research activities under approved protocols .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating clinical research activities, including patient recruitment, data collection, and compliance with regulatory standards. Proficient in evaluating clinical data and ensuring adherence to research protocols.
Highest-signal resume keywords
Clinical Research CoordinationPatient Recruitment and EnrollmentData Collection and AnalysisRegulatory ComplianceClinical Research Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Biological Sample ProcessingStandardized Diagnostic TestingClinical Data AnalysisMedical Terminology KnowledgeProtocol Compliance Evaluation
Soft Skills
Patient EducationCommunication SkillsInterpersonal Skills
Tools & Technologies
Microsoft Software Applications
Certifications & Qualifications
Clinical Research Certification
Industry Keywords
IRB ComplianceFDA RegulationsQuality AssuranceClinical Research ProtocolsImaging Methodologies
About the role
Key responsibilities & impact- Coordinate and perform daily clinical research activities under approved protocols
- Assess patient records to identify eligible research participants
- Recruit, interview, enroll, and obtain informed consent from patients
- Educate patients and families about clinical study purposes, goals, and processes
- Coordinate patient care appointments, procedures, and diagnostic testing
- Collect, process, and evaluate biological samples
- Administer, evaluate, and calculate standardized diagnostic testing or questionnaire scores
- 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
- Coordinate and prepare for external quality assurance and control reviews
- Participate in developing 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
- A pre-employment physical, including a drug screen, may be required
- Experience or knowledge in imaging methodologies preferred
- Knowledge of medical terminology desired
- Clinical research certification from an accredited certifying agency desired
- Experience using Microsoft Software applications desired
Benefits
Comp & perks- Regular position
- Full-time schedule (40 hours per week)
- Hybrid work arrangement
- Equal opportunity employment, including veterans and disability