Clinical Research Coordinator - Ccc | Clinical Trials Office
The Ohio State University
Columbus, US
Perform daily clinical research activities
Assess patient records for eligibility
Obtain informed consent from patients
The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office (CTO) within the Comprehensive Cancer Center
Job Summary
The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office (CTO) within the Comprehensive Cancer Center.
Responsibilities include assessing patient eligibility, obtaining informed consent, coordinating patient care, monitoring for adverse reactions, and ensuring regulatory compliance.
The Ohio State University offers excellent professional development opportunities, including support for certifications, career advancement, and a Master of Clinical Research degree program.
Matching Summary
The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office (CTO) within the Comprehensive Cancer Center.
Skills & Requirements
Must-have
Perform daily clinical research activities
Assess patient records for eligibility
Obtain informed consent from patients
Coordinate patient care appointments
Monitor patients for adverse reactions
Collect and enter clinical research data
Ensure regulatory compliance (IRB, FDA)
Nice-to-have
Strong communication skills
Flexibility and adaptability
Professional development support
Career growth opportunities
Key Requirements
Bachelor's Degree in related field or equivalent experience