| Duration | 10, 5, 2 |
|---|---|
| Sessions | 12 Sessions , 1 Assessments |
| Course Location: | Recorded |
|
Type of the Activity |
Recorded Educational Content
Accessibility |
|
Topic |
Duration |
|
Course Introduction |
3 minutes |
|
Session 1: Research Acronyms & Terminology |
58 min |
|
Session 2: Overview / phases of clinical research |
29 min |
|
Session 3: Ethical consideration during clinical trial |
48 min |
|
Session 4: Good Clinical Practice (GCP) overview |
22 min |
|
Session 5: Infrastructure Requirements of Clinical Research |
1 hour |
|
Session 6: part1: How to select clinical trial and initiate it? |
40 min |
|
Session 7: part2: How to select clinical trial and initiate it? |
42 min |
|
Session 8: Data Management |
1 hour 8 min |
|
Session 9: part 1: Publication process |
22 min |
|
Session 10: part 2: Publication process |
24 min |
|
Session 11: part 3: Publication process |
41 min |
1. Review the process of planning, developing, and executing
a research project.
2. list different research designs and the basis for selecting one over the other.
3. Define the research proposal and its components.
4. Explain methods of designing and analyzing surveys.
5. Identify the necessary skills in using standard
supporting software.
Join this self-paced course to gain knowledge about research from a highly qualified individual.
This course is one of the required courses for all Saudi Board Training Programs by the Saudi Commission for Health Specialities.
1. By the end of this module, learners will be able to:
Define and explain key acronyms and terminology used in clinical research.
Describe the overview and phases of clinical research, from concept to completion.
Identify and apply the ethical considerations involved during clinical trials.
Explain the principles and importance of Good Clinical Practice (GCP).
Recognize the infrastructure requirements necessary to conduct effective clinical research.
Demonstrate understanding of how to select and initiate a clinical trial.
Outline the processes involved in data management within clinical research.
Discuss the publication process and dissemination of clinical trial findings.
you have to attend 60% of the course and fill up the survey to obtain the certificate>
