Clinical Trials Research Coordinator I

Cleveland Clinic; Cleveland (OH); On-site; USD 29,000 - 44,000; Full time

Job summary

Cleveland Clinic's Main Campus seeks a Research Coordinator I to enroll patients in clinical trials, conduct study visits and collect questionnaires, ensuring high-quality data and protocol compliance.

You will coordinate regulatory documents, manage data, communicate with sponsors and monitors, schedule visits, and support investigators in executing protocols while maintaining patient safety and study integrity.

Qualifications

• Two years of clinical research or healthcare experience.
• OR Associate's or Bachelor's degree in healthcare or science.
• Proficient with word processing, spreadsheets, databases, presentation software, data entry, and EPIC.
• Understanding of basic study design.
• Within 90 days of hire, complete certification in Human Subjects Research as required.

Responsibilities

• Coordinate the compliant implementation and conduct of human subject research projects.
• Maintain regulatory documents and binders, conduct data management, complete IRB submissions and communicate with the research team.
• Report and document serious adverse events and safety logs.
• Communicate with sponsors, monitors and research personnel to ensure study compliance.
• Collaborate with investigators, sponsors and research staff to plan and evaluate protocols, including recruitment.
• Schedule pre-site visits, site initiation visits, webinars and monitoring/close-out visits.
• Plan and evaluate project protocols and recruitment.
• Monitor and report project status and research data.
• Complete regulatory documents, data capture and monitoring plans.
• Assist with audits and maintain research tools.
• Complete certification in Human Subjects Research as required.

Skills

Clinical research

Regulatory knowledge

Data management

Communication skills

Education

High School Diploma or GED

Associate's or Bachelor's Degree in Healthcare/Science

Tools

EPIC

Job description

Cleveland Clinic's Main Campus seeks a Research Coordinator I to enroll patients in clinical trials, conduct study visits and collect questionnaires, ensuring high-quality data and protocol compliance.

You will coordinate regulatory documents, manage data, communicate with sponsors and monitors, schedule visits, and support investigators in executing protocols while maintaining patient safety and study integrity.