MS Neurology Clinical Research Coordinator III

University of Florida; Gainesville (FL); On-site; USD 60,000 - 70,000; Full time

Job summary

University of Florida in Gainesville seeks a Clinical Research Coordinator III in Neurology, Division of General Neurology, MS subdivision, to oversee daily trial operations and regulatory submissions. The role emphasizes informed consent, subject coordination, and data integrity across trials.

The ideal candidate has three years of human subject research experience, familiar with IRB processes and NIH/FDA procedures, and can coordinate with investigators and sponsors to ensure compliant trial

Qualifications

• Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
• Three years of human subject research experience and familiarity with clinical trial processes is expected.
• Knowledge of NIH and FDA procedures and regulatory requirements is preferred.

Responsibilities

• Coordinate protocol subjects and manage testing, scheduling, and consent processes.
• Review medical data, enter information into sponsor case report forms, and ensure data integrity.
• Ensure regulatory documentation, submissions, continuing reviews, and revisions are completed per IRB requirements.
• Attend meetings and communicate with investigators, staff, and sponsors to support trial conduct.
• Monitor compliance, QA activities, and adverse event reporting as required.

Skills

Clinical research

Regulatory compliance

Communication

Education

Bachelor's degree

Tools

Microsoft Office

CTMS

Job description

University of Florida in Gainesville seeks a Clinical Research Coordinator III in Neurology, Division of General Neurology, MS subdivision, to oversee daily trial operations and regulatory submissions. The role emphasizes informed consent, subject coordination, and data integrity across trials.

The ideal candidate has three years of human subject research experience, familiar with IRB processes and NIH/FDA procedures, and can coordinate with investigators and sponsors to ensure compliant trial