This is a an online self-paced course that is accessible 24/7 for 2 weeks starting from the date of enrollment.
Certificate of attendance is provided upon completion of the course requirements.
Course Duration:
- Accessible for 2 weeks
One of the required courses by SCFHS for Saudi Board Training Programs
Target Audience: All Healthcare Practitioners
Speaker: Dr.Nagham Sheblaq. Msc, BSc. Pharma, certified Clinical Research Professional (CCRP), CCRPh
Course Objectives:
- Review the process of planning, developing, and executing a research project.
- list different research designs and the basis of selecting one over the other.
- Define the research proposal and its components.
- Explain methods of designing and analyzing surveys.
- Identify the necessary skills in using standard supporting software.
Course Topics:
|
Topic |
Objective |
| Research Acronyms & Terminology | Review commons terminology and acronyms used in clinical research |
| Overview / phases of clinical research | Define what is clinical trial
Discuss types of clinical trials and designs Selecting a study design Research Hypothesis Selection of endpoints |
| Ethical consideration during clinical trial | Ethical issues related to subjects
Ethical issues related to particular research approaches Ethics and professionalism |
| Good Clinical Practice (GCP) overview | Gain familiarity with the structure and content of regulations and guidelines governing clinical trials. |
| Infrastructure Requirements of Clinical Research | Investigator, Qualifications and responsibilities
Research team members roles and responsibilities |
| How to select clinical trial and initiate it? | Provide tips on how to evaluate and select clinical trials
Discuss practical steps of how to initiate study Components of Research Protocol |
| Data Management
|
How to collect/ manage collected clinical data
Data Entry Analysis/ management requirements |
| Publication process | Academic Medical Writing (Abstract, Poster)
Academic Medical Writing (Manuscript) The Scientific Journal Publication Process |
-
Course Content
- Course Introduction
- Lecture 1: Research Acronyms & Terminology
- Lecture 2: Overview / phases of clinical research
- Lecture 3: Ethical consideration during clinical trial
- Lecture 4: Good Clinical Practice (GCP) overview
- Lecture 5: Infrastructure Requirements of Clinical Research
- Lecture 6 Part 1: How to select clinical trial and initiate it?
- Lecture 6 Part 2: How to select clinical trial and initiate it?
- Lecture 7: Data Management
- Lecture 8 Part 1: Publication process
- Lecture 8 Part 2: Publication process
- Lecture 8 Part 3: Publication process
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End of Course assessment
