Clinical Research Coordinator — On-Site Trials

The Ohio State University; Columbus (OH); On-site; USD 55,000 - 75,000; Full time

Job summary

The Ohio State University is seeking a Clinical Research Coordinator Float with the Clinical Trials Management Office in Medicine to coordinate daily clinical research activities. The role supports multiple COM departments and requires on-site work across locations.

Responsibilities include recruiting and consenting patients, data collection and regulatory compliance, with prior clinical research experience and a Bachelor’s degree.

Qualifications

• Bachelor’s degree in biological, health or related field or equivalent combination of education and experience.
• One year of clinical research experience required.
• Background check and possible pre-employment physical/drug screen.

Responsibilities

• Coordinate and perform daily clinical research activities per approved protocols.
• Recruit, screen, and enroll patients; obtain informed consent.
• Monitor patient safety and adverse events; notify appropriate staff.
• Collect, process and analyze data; ensure data integrity.
• Coordinate regulatory compliance with IRB, FDA and sponsors.

Skills

Clinical research

IRB compliance

Data collection

Regulatory knowledge

Education

Bachelor’s degree in biological sciences

Tools

REDCap

Medidata

Microsoft Office

Job description

The Ohio State University is seeking a Clinical Research Coordinator Float with the Clinical Trials Management Office in Medicine to coordinate daily clinical research activities. The role supports multiple COM departments and requires on-site work across locations.

Responsibilities include recruiting and consenting patients, data collection and regulatory compliance, with prior clinical research experience and a Bachelor’s degree.