Clinical Research Coordinator: Lead Studies & Patient Enrollment

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 48,000 - 76,000; Full time

Job summary

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to support daily study activities under approved protocols in a university hospital setting.

You will screen records for eligibility, obtain informed consent, schedule visits, collect data, manage regulatory documents, and ensure adherence to sponsor requirements. A Bachelor's degree in biological or medical fields is required; 0–4 years of relevant experience preferred.

Qualifications

• Bachelor’s Degree in Biological Sciences, Health Sciences or medical field required.
• 0 years of relevant experience required; 2-4 years preferred.
• Final candidates subject to background check; drug screen or physical may be required.

Responsibilities

• Implements, coordinates and performs daily clinical research activities per protocols.
• Assists in identifying eligible patients and enrolling participants; obtains informed consent.
• Schedules surgeries, procedures, and diagnostic tests; manages follow-up visits.
• Collects and documents medical histories; coordinates and documents care of patients.
• Evaluates patient responses for adverse events; notifies appropriate staff; ensures regulatory compliance.
• Maintains regulatory documents and prepares case report forms; supports external QA/reviews.
• Attends meetings and contributes to protocol development and data collection.
• Gathers and organizes data for analysis and publication.

Skills

Clinical research coordination

Patient recruitment

Regulatory compliance

Education

Bachelor’s Degree in Biological Sciences, Health Sciences or medical field

Job description

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to support daily study activities under approved protocols in a university hospital setting.

You will screen records for eligibility, obtain informed consent, schedule visits, collect data, manage regulatory documents, and ensure adherence to sponsor requirements. A Bachelor's degree in biological or medical fields is required; 0–4 years of relevant experience preferred.