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MedStar Health is proud to be participating in The Introduction to the Principles and Practice of Clinical Research (IPPCR) course established by the National Institutes of Health (NIH). The program provides training in designing a successful clinical trial by focusing on biostatistical and epidemiologic methods, study design, protocol preparation, patient monitoring, quality assurance, ethical and legal issues, and more. Other areas covered are data management and ethical issues, including protection of human subjects. This course will be of interest to resident and fellow physicians, as well as junior level faculty, wishing to enhance their understanding and expertise in clinical research.
The course will be conducted entirely online in a self-paced format. However, it is recommended that participants view 1 to 2 lectures per week to give themselves ample time to understand the theoretical and practical aspects of the content and to prepare for the final examination. The course is composed of approximately 40 lectures, and participants should plan for approximately 50 hours to watch the video-archived lectures, and additional time for course readings, discussion board participation, and the online multiple choice final examination. The course schedule is attached.
This course is being offered as a certificate program. At the conclusion of the course, a written examination is required for the certificate to be granted. Registration is required in order for you to be eligible to take the examination and receive certification.
Textbook: The course textbook, Principles and Practice of Clinical Research, Third Edition, will be provided to residents and fellows who register for the course, via their local GME office. Residents and fellows who complete the course and receive certification may keep the textbook. Those who do not complete the course certification must return the book to the GME office or reimburse the cost of $90 per book.
- 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
The 2017-2018 course schedule, syllabus and additional information are available online: https://clinicalcenter.nih.gov/training/training/ippcr1.html.
If you are interested in registering, please visit this website (you are registering as a remote site participant): https://ippcr.nihtraining.com/register.php?remote_site=true.
- For organization please choose: MedStar Health, Department of Graduate Medical Education/Columbia, MD.
- If asked for title, or in the “other” field, please specify: resident/fellow, faculty, medical student.