Courses / Recorded courses

Research Methodology and Statistics Course (Recorded Educational Content Accessibility)

Accessibility Duration
115.00 SAR
70 Users Registered
Learning Activity details
Duration 10, 5, 2
Sessions 12 Sessions , 1 Assessments
Course Location: Recorded
Select The Dates Of The Updated Scientific Valid Content Released By The Scientific Committee.


Learning Activity Agenda:


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

 











Scientific Committee:

Target Audience:
  • All

Learning Activity Objectives:

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.


Learning Activity Description:

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. 


Learning Outcome:

1.       Research  Acronyms & Terminology

2.       Overview / phases of clinical research

3.       Ethical consideration during clinical trial

4.       Good Clinical Practice (GCP) overview

5.       Infrastructure Requirements of Clinical Research

6.       How to select clinical trial and initiate it?

7.       Data Management

8.       Publication process



Certificates

you have to attend 60% of the course and fill up the survey to obtain the certificate>



Learning Activity requirements:



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