STEMM Jobs

Clinical Research Coord I-Epilepsy Division

  • University of Florida
  • United States
  • May 29, 2026
Science Full Time - Continuing

  •  

    About University of Florida
    At the University of Florida, we are a people of purpose. We're committed to challenging convention and ourselves. We see things not as they are, but as they could be. And we strive for a greater impact: one measured in people helped...

    Job Description:

    Classification Title:

    Clinical Research Coord I
    Classification Minimum 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
    Job Description:
    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.

    Clinical Research Coordination:

    • Screen, recruit, consent, and enroll research participants in accordance with IRBapproved 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

    Data Collection and Management:

    • 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

    Research Operations and Administrative Support:

    • 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
    Regulatory and Compliance Support:
    • 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
    Expected Salary:

    $46,000 - $52,000 Annually
    Required Qualifications:

    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
    Preferred:
    Special Instructions to Applicants:

    In order to be considered, you must upload your cover letter and resume.

    Application must be submitted by 11:55 p.m. (ET) of the posting end date.
    Health Assessment Required: Yes



  •  or Save this Job
    • col-narrow-left   

    Job ID:

    43022

    Location:

    Gainesville 

    Field:

    Science
    col-narrow-right   

    Job Views:

    49

    Employment Type:

    Full Time - Continuing
    col-wide   

    Job Description:

    "\n\n\n\n\n\n\n\n\n\n
    Classification Title:<\/th>\n\n

    Clinical Research Coord I<\/p>\n<\/td>\n<\/tr>\n

    Classification Minimum Requirements:<\/th>\n\n

    Associate\u2019s 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<\/p>\n<\/td>\n<\/tr>\n

    Job Description:<\/th>\n\n
    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<\/div>\n
    closely with the Principal Investigator and research team to ensure efficient, compliant, and timely implementation of study protocols.<\/div>\n

    Clinical Research Coordination:<\/strong><\/p>\n

      \n
    • Screen, recruit, consent, and enroll research participants in accordance with IRBapproved protocols and regulatory guidelines<\/li>\n
    • Coordinate and schedule study visits, including procedures involving MEG, MRI, questionnaires, and clinical data collection<\/li>\n
    • Maintain communication with study participants and support participant retention<\/li>\n<\/ul>\n

      Data Collection and Management:<\/strong><\/p>\n

        \n
      • Collect, enter, review, and manage study data using REDCap and related databases<\/li>\n
      • Ensure data integrity, completeness, and adherence to protocol requirements<\/li>\n
      • Maintain study records, source documentation, and regulatory binders in compliance with institutional standards<\/li>\n<\/ul>\n

        Research Operations and Administrative Support:<\/strong><\/p>\n

          \n
        • \n
          Track study progress, enrollment, and timelines to meet project goals<\/div>\n<\/li>\n
        • \n
          Assist with preparation of research-related materials, including abstracts,<\/div>\n
          manuscripts, and grant documents<\/div>\n<\/li>\n
        • \n
          Coordinate activities among investigators, clinical staff, and research<\/div>\n<\/li>\n<\/ul>\n
          Regulatory and Compliance Support:<\/strong><\/div>\n
            \n
          • \n
            Assist with preparation and submission of IRB applications, amendments, and<\/div>\n
            continuing reviews.<\/div>\n<\/li>\n
          • \n
            Ensure compliance with federal regulations, UF policies, and Good Clinical<\/div>\n
            Practice (GCP) guidelines<\/div>\n<\/li>\n
          • \n
            Support study monitoring, audits, and regulatory inspections as needed<\/div>\n<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n
    Expected Salary:<\/th>\n\n

    $46,000 - $52,000 Annually<\/p>\n<\/td>\n<\/tr>\n

    Required Qualifications:<\/th>\n\n

    Associate\u2019s 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<\/p>\n<\/td>\n<\/tr>\n

    Preferred:<\/th>\n <\/td>\n<\/tr>\n
    Special Instructions to Applicants:<\/th>\n\n

    In order to be considered, you must upload your cover letter and resume.<\/p>\n

    Application must be submitted by 11:55 p.m. (ET) of the posting end date.<\/p>\n<\/td>\n<\/tr>\n

    Health Assessment Required:<\/th>\nYes<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

    <\/p>"

    Posted:

    29/05/2026