Neurology Research Administration Management Analyst 3

Ohio State University - Columbus, OH

Full-time - Mid Level

Columbus, OH

Educational Services

About the position

The Neurology Research Administration Management Analyst 3 position at Ohio State University Wexner Medical Center involves managing research administration within the Department of Neurology, specifically collaborating with the Division of Health Services Research. The role encompasses leading division meetings, supporting research activities, overseeing project execution, and ensuring compliance with established protocols. The analyst will also be responsible for training team members and serving as a liaison between researchers and clinical staff.

Responsibilities

• Manage division-related activities and set agendas for meetings.
• Support the division in specific activities such as conferences.
• Draft and revise research protocols and complete IRB submissions.
• Review protocols for adherence to established Standard of Care.
• Coordinate and execute research projects in accordance with approved protocols.
• Draft data collection forms and research materials.
• Participate in data acquisition and recruitment/retention processes.
• Evaluate patient compliance related to research protocols.
• Develop plans to meet requirements of new studies/protocols.
• Organize and prepare for external quality assurance and control reviews.
• Develop and implement training needs required by sponsors.
• Assist in training students, residents, and fellows on clinical research processes.
• Lead protocol-specific in-services for the research team.
• Work with finance and billing offices to track research invoicing.
• Serve as a resource for team members, PIs, and administration.
• Act as the primary liaison between researchers and clinical staff.
• Attend training conferences, seminars, and study-related meetings.
• Lead and implement process improvement projects for the Division.

Requirements

• Bachelor's Degree or equivalent combination of training and experience required.
• Experience in a clinical research capacity conducting clinical research studies preferred.
• Clinical research certification from ACRP or SoCRA desired or planned.

Nice-to-haves

• Experience with IRB submissions and protocol reviews.
• Familiarity with clinical research regulations and processes.

Benefits

• Health insurance coverage
• Paid holidays
• Tuition reimbursement
• Professional development opportunities