Cancer Trials Clinical Research Coordinator

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 52,000 - 75,000; Full time

Job summary

The Ohio State University Wexner Medical Center in Columbus seeks a Clinical Research Coordinator to support daily clinical research activities within the Comprehensive Cancer Center’s trials program. You will coordinate patient screening, consent, scheduling, and data collection under IRB guidance.

The role emphasizes regulatory compliance, accurate documentation, and collaboration with investigators, clinical staff, and sponsors to advance cancer research.

Qualifications

• Bachelor’s degree in biological sciences, health sciences, social sciences, or related field.
• At least 1 year of clinical research experience is required.
• Knowledge of medical terminology desired and clinical research certification desired.
• Proficiency with Microsoft Office software and clear written and oral communication.

Responsibilities

• Assist in identifying eligible patients from records for participation in protocols.
• Recruit, interview and enroll patients and obtain informed consent.
• Coordinate scheduling of visits and tests according to the protocol.
• Monitor patient responses and report adverse events to care teams and sponsors.
• Document data and ensure IRB and sponsor regulatory compliance.
• Assist with data extraction, coding and analysis for study purposes.
• Support development of new protocols and contribute to study goals.

Skills

Clinical research

Regulatory knowledge

Data collection/analysis

Communication skills

Education

Bachelor’s degree in biological sciences or related field

Tools

Microsoft Office

Job description

The Ohio State University Wexner Medical Center in Columbus seeks a Clinical Research Coordinator to support daily clinical research activities within the Comprehensive Cancer Center’s trials program. You will coordinate patient screening, consent, scheduling, and data collection under IRB guidance.

The role emphasizes regulatory compliance, accurate documentation, and collaboration with investigators, clinical staff, and sponsors to advance cancer research.