CLINICAL RESEARCH INFORMATICS

BMI/POPHLTH 694

Provides an introduction to key concepts, methods, and tools of biomedical and health informatics used in precision medicine and population health, with emphasis on collection, management, and analysis of real-world data.

BMI 901

Become familiar with basic informatics principles and techniques to support clinical research. Content includes information systems for protocol design; regulatory compliance; approaches for patient recruitment; efficient protocol management; data collection and acquisition; data security, storage, transfer, processing and analysis.

BMI 573

Familiarize students with basic informatics principles and techniques to support clinical research and quality improvement studies from a perspective of data-driven approaches. Content includes information systems for study design; regulatory compliance; use of electronic health records data for research; data collection and acquisition; data security, storage, transfer, processing and analysis.

BMI/MEDICINE 918

Biomedical Informatics is an interdisciplinary field that combines knowledge of information sciences and medical sciences to optimize the use and application of biomedical data across the spectrum from molecules to individuals to populations. Offers an overview of the field of health informatics by providing students with the fundamental knowledge of the concepts of health informatics and how technology can be used in the delivery of health care.

BMI 544

Practical training and skills required in clinical and healthcare research; design, implementation, and conduct of clinical trials and health services research studies; protocol and informed consent development using protocol templates; regulatory requirements; human subjects research protections considerations; data and safety monitoring plans; data collection strategies and data management; strategies to recruit/retain diverse and equitable study participants; research study agreements; budget development and justification; federal, institutional, and sponsor-defined requirements; establishment of research infrastructures for participant safety and study success; preparation of investigator-INDs/IDEs; and investigator responsibilities.