- Provide an overview of basic biostatistical and epidemiologic methods involved in conducting clinical research.
- Describe the principles involved in the ethical, legal, and regulatory issues in clinical human subjects research, including the role of Institutional Review Boards (IRBs).
- Describe principles and issues involved in monitoring patient-oriented research.
- Describe the infrastructure required in performing clinical research and the steps involved in developing and funding research studies.
Introduction to the Principles and Practice of Clinical Research (IPPCR)
National Institutes of Health via Independent
Overview
Coursera Spring Sale
40% Off Coursera Plus Annual!
Grab it
The Introduction to the Principles and Practice of Clinical Research (IPPCR) course trains participants on how to effectively and safely conduct clinical research. The course focuses on the spectrum of clinical research and the research process by highlighting biostatistical and epidemiologic methods, study design, protocol preparation, patient monitoring, quality assurance, ethical and legal issues, and much more. This course will be of interest to physicians, scientists, medical and dental students, nurses, public health professionals, and others conducting or planning a career in clinical research.
Syllabus
- Module 1: Introduction to Clinical Research
- Module 2: Statistics in Clinical Research
- Module 3: Practical Considerations for Implementation
- Module 4: Selection of Study Participants
- Module 5: Writing the Protocol & Protocol Implementation
- Module 6: Safety Review & Monitoring
- Module 7: Data Quality & Results Reporting
Taught by
John I. Gallin, Lisa Cordes, Lisa Cordes, and Anne Zajicek