Clinical Research Coordinator — Cancer Control Trials

The Ohio State University; Columbus (OH); On-site; USD 40,000 - 65,000; Full time

Job summary

The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Solove Research Institute invites applications for a Clinical Research Coordinator in Cancer Control. The role supports daily research activities, patient recruitment, consent, and data handling within the Clinical Trials Office.

Collaboration with clinical staff and sponsors is essential. Ideal candidates hold a biology/health sciences degree and have clinical research exposure, with strong communication

Qualifications

• Bachelor’s degree in biological, health, social sciences or a related field.
• Minimum of 1 year clinical research experience.
• Knowledge of medical terminology.
• Effective communication with staff and participants is required.

Responsibilities

• Assist with daily clinical research activities and protocol compliance.
• Recruit, interview and enroll patients in protocols.
• Obtain informed consent and ensure regulatory compliance.
• Educate patients and families on study purpose, goals and processes.
• Coordinate scheduling and follow-up of patient care appointments and testing per protocol.
• Monitor patients for adverse reactions and escalate as needed.
• Document unfavorable responses and notify sponsors and regulatory bodies.
• Assist with collecting, extracting, coding and analyzing data.
• Ensure compliance with IRB, FDA and sponsor regulations; prepare for external reviews.
• Contribute to development of new research protocols and study goals.

Skills

Communication skills

Clinical research

Medical terminology

Microsoft Office

Education

Bachelor’s degree in biological/health/social sciences or related field

Tools

Microsoft Office Suite

Job description

The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Solove Research Institute invites applications for a Clinical Research Coordinator in Cancer Control. The role supports daily research activities, patient recruitment, consent, and data handling within the Clinical Trials Office.

Collaboration with clinical staff and sponsors is essential. Ideal candidates hold a biology/health sciences degree and have clinical research exposure, with strong communication