Clinical Research Coord I-Epilepsy Division
University of Florida•Gainesville, FL
•Onsite
About The Position
The Clinical Research Coordinator I will support clinical research activities within the iBRAIN Laboratory in the Department of Neurology at the University of Florida. This position is responsible for coordinating human subjects research focused on neurological disorders, including epilepsy and dementia. The incumbent will work closely with the Principal Investigator and research team to ensure efficient, compliant, and timely implementation of study protocols.
Requirements
- Associate’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience
Nice To Haves
- Experience with REDCap and related databases
- Familiarity with Good Clinical Practice (GCP) guidelines
- Experience coordinating human subjects research focused on neurological disorders, including epilepsy and dementia
Responsibilities
- Screen, recruit, consent, and enroll research participants in accordance with IRB-approved protocols and regulatory guidelines
- Coordinate and schedule study visits, including procedures involving MEG, MRI, questionnaires, and clinical data collection
- Maintain communication with study participants and support participant retention
- Collect, enter, review, and manage study data using REDCap and related databases
- Ensure data integrity, completeness, and adherence to protocol requirements
- Maintain study records, source documentation, and regulatory binders in compliance with institutional standards
- Track study progress, enrollment, and timelines to meet project goals
- Assist with preparation of research-related materials, including abstracts, manuscripts, and grant documents
- Coordinate activities among investigators, clinical staff, and research
- Assist with preparation and submission of IRB applications, amendments, and continuing reviews.
- Ensure compliance with federal regulations, UF policies, and Good Clinical Practice (GCP) guidelines
- Support study monitoring, audits, and regulatory inspections as needed
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
