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Job summary
A medical research organization in Columbia, South Carolina, is seeking a skilled Clinical Research Coordinator. This role involves managing the daily operations of clinical trials, ensuring compliance with regulations, and maintaining high patient safety standards. Ideal candidates should have 2–3 years of experience in clinical research coordination and a Bachelor’s degree in a relevant field. CCRC or CCRP certification is preferred. Strong organizational skills and proficiency with EDC systems are essential.
Qualifications
2–3 years of experience in clinical research coordination.
Bachelor’s degree in a life science, healthcare, or related field is required.
CCRC or CCRP certification is highly preferred.
Responsibilities
Oversee the lifecycle of clinical trials from site initiation to close-out.
Screen and enroll eligible study participants and maintain retention.
Ensure timely entry of Case Report Forms and maintain regulatory binders.
Skills
Clinical trial management
Patient recruitment and retention
Data entry and regulatory compliance
Phlebotomy
Organizational skills
Education
Bachelor’s degree in a life science or related field
CCRC or CCRP certification
Tools
Electronic Data Capture (EDC) systems
Electronic Medical Records (EMR) platforms
Job description
A medical research organization in Columbia, South Carolina, is seeking a skilled Clinical Research Coordinator. This role involves managing the daily operations of clinical trials, ensuring compliance with regulations, and maintaining high patient safety standards. Ideal candidates should have 2–3 years of experience in clinical research coordination and a Bachelor’s degree in a relevant field. CCRC or CCRP certification is preferred. Strong organizational skills and proficiency with EDC systems are essential.