The Biomedical Informatics and Data Science (BIDS) Program, housed in the Department of Health Outcomes and Biomedical Informatics and closely affiliated with the Clinical and Translational Science Institute (CTSI), conducts various informatics research and service across the University of Florida. Service initiatives include supporting the informatics infrastructure for the CTSI, the OneFlorida+ Clinical Research Network, and the UF Health Cancer Center (UFHCI).
Research Project Management and Protocol Implementation: Develop project plans in collaboration with investigators. Coordinate multiple research projects, including multi-site studies, led by BMI faculty. Track project objectives, milestones, deliverables, status reports, study results to ensure research activities remain on schedule. Translate study design decisions into concrete tasks, and facilitate setting implementation priorities. Create and maintain budgets and project spending. Lead the development and maintenance of IRB protocols, project objectives, and other research-related tasks and documentation. Serve as a liaison for human subjects’ payments. Handle protected health information and human subjects’ issues with sensitivity. Coordinate roles, responsibilities, and interdependencies of research team members, including students. Manage communication among staff, study sponsors, healthcare professionals, and investigators, to ensure on-time reports and other deliverables. Work with investigators and administrative staff to maintain budgets, monitor project spending, and develop and maintain IRB protocols, and other research-related documentation.
Conduct all phases of research including study recruitment, informed consent, retention, implementation, and data collection and analysis. Communicate with study participants to address participant questions/issues and implement study protocols.
Communication: Organize, lead, and document research project team meetings. Track and communicate project updates to team members, leadership, department administration, and other internal and external stakeholders. Manage communication among staff, study sponsors, healthcare professionals, and investigators. Communicate with the IRB Privacy Office, and other regulatory bodies to obtain and maintain all necessary regulatory approval.
Coordinate research proposal development: Collaboratively manage submission milestones and deadlines. Identify and review extramural funding opportunities and share opportunities with investigators and other partners.
Supervise activity of research staff members in support of assigned projects and initiatives.
Dissemination: Work with Investigators to produce publications in peer-reviewed journals and presentations to academic, organizational, and community audiences. Lead tracking publications and facilitate research product dissemination.