This free, self-paced course will provide information on many aspects of clinical research including the scientific process, research protocol, documentation, regulatory documents, adverse event classification, and reporting events to regulatory bodies. Record retention, drug accountability, and study closure are also discussed in this course, which is intended primarily for health care workers and teams in a biocontainment unit environment. Additional medical staff and public health professionals may also find the course to be of benefit, including medical and/or nursing staff, administration, education/training leadership, and infection control leadership. Staff specializing in communications, specialized clinical areas, laboratory, facilities management, and environmental services are also welcome.
Access enrollment information here.