Clinical Research Coordinator: Study Operations & Patient Care

Wexner Medical Center; Columbus (OH); On-site; USD 50,000 - 70,000; Full time

Job summary

Wexner Medical Center in Columbus, OH seeks a Clinical Research Coordinator to implement daily research activities under approved protocols and to assist with patient eligibility assessment and enrollment. The role involves coordinating visits, scheduling procedures, and documenting medical histories in study records.

The position supports regulatory compliance with IRB/FDA and sponsors, handles data collection and basic manuscript preparation, and participates in protocol development and team

Qualifications

• Bachelor's Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
• 0 years of relevant experience required.
• 2-4 years of relevant experience preferred.

Responsibilities

• Implements, coordinates and performs daily clinical research activities in accordance with approved protocols.
• Assists with assessing patient records to identify eligible participants and enrolls them after informed consent.
• Collects and documents medical histories and coordinates scheduling and follow-up for participants.
• Participates in collection, processing and evaluation of biological samples and related data.
• Ensures compliance with IRB, FDA, and sponsor requirements; prepares regulatory documents and case report forms.
• Attends departmental meetings and contributes to development of study protocols and processes.

Skills

Clinical research coordination

Data management

Patient enrollment

Education

Bachelor's degree in Biological/Health Sciences or medical field

Job description

Wexner Medical Center in Columbus, OH seeks a Clinical Research Coordinator to implement daily research activities under approved protocols and to assist with patient eligibility assessment and enrollment. The role involves coordinating visits, scheduling procedures, and documenting medical histories in study records.

The position supports regulatory compliance with IRB/FDA and sponsors, handles data collection and basic manuscript preparation, and participates in protocol development and team