| Duration | |
|---|---|
| Sessions | |
| Course Location: | Live |
|
Day 1 (20 January 2024) |
|||
|
Session 1 |
6:00 pm – 6:15 pm |
An overview of the
program |
Dr. Samaa AL Tabbah |
|
Session 2 |
6:15 pm – 6:40 pm |
Scientific Research:
Process and Terminology |
|
|
Session 3 |
6:40 pm – 7:00 pm |
Research Question
Formulation |
|
|
Session 4 |
7:00 pm – 8:00 pm |
Literature Search and
Reference Management |
|
|
Coffee Break |
8:00 pm – 8:10 pm |
Coffee Break |
|
|
Session 5 |
8:10 pm – 8:25 pm |
Observational Study
Designs |
|
|
Session 6 |
8:25 pm – 8:45 pm |
Experimental Study
Designs |
|
|
Session 7 |
8:45 pm – 9:00 pm |
Introduction to
Biostatistics |
|
|
Close-Up |
9:00 pm – 9:15 pm |
Wrap-up and closing |
|
|
Day 2 |
|||
|
Session 1 |
6:00 pm – 6:15 pm |
Review of Day 1 |
Dr. Nagham Ramzi |
|
Session 2 |
6:15 pm – 6:40 pm |
Basics of Scientific
Writing |
|
|
Session 3 |
6:40 pm – 7:00 pm |
Scientific Article
Writing |
|
|
Session 4 |
7:00 pm – 8:00 pm |
Regulatory Documents
Writing |
|
|
Coffee Break |
8:00 pm – 8:10 pm |
Coffee Break |
|
|
Session 5 |
8:10 pm – 8:25 pm |
Scientific Journal Basic
Info and Selection |
|
|
Session 6 |
8:25 pm – 8:45 pm |
Process of journal
submission |
|
|
Session 7 |
8:45 pm – 9:00 pm |
Replying to reviewers’
comments and resubmission |
|
|
Close-Up |
9:00 pm – 9:15 pm |
Wrap-up and closing |
Dr. Samaa AL Tabbah |
Goal 1: Enhance Participants' Understanding
of Clinical Research
Goal 2: Develop Participants' Research
Design Skills
Goal 3: Improve Participants' Data Analysis
Proficiency
Goal 4: Promote Ethical Conduct in Clinical
Research
Goal 5: Strengthen Participants' Critical
Appraisal Skills
Goal 6: Enhance Participants' Communication
and Publishing Abilities
Goal 7: Provide a Comprehensive Understanding
of the Clinical Research Process
Navigating Clinical Research: From Concept to Publication two-day course for all healthcare practitioners.
Topics of the course:
1-
Scientific Research:
Process and Terminology
2-
Research Question
Formulation
3-
Literature Search and
Reference Management
4-
Observational Study Designs
5-
Experimental Study Designs
6-
Introduction to
Biostatistics
7-
Basics of Scientific
Writing
8-
Scientific Article Writing
9-
Regulatory Documents
Writing
10-
Scientific Journal Basic
Info and Selection
11-
Process of journal submission
12-
Replying to reviewers’
comments and resubmission
1. Formulate research questions and
hypotheses that are relevant to clinical practice and can be investigated
through research.
2. Design robust research studies,
including selecting appropriate study designs, sampling methods, and data
collection strategies.
3. Analyse research data using relevant
statistical techniques and interpret the results accurately.
4. Adhere to ethical principles in clinical
research, including obtaining informed consent, ensuring participant privacy,
and handling data responsibly.
5. Navigate regulatory requirements, such
as Institutional Review Board (IRB) approval and compliance with relevant laws
and guidelines.
6. Critically evaluate and appraise
scientific literature, identifying strengths and weaknesses in study design and
methodology.
7. Communicate research findings
effectively through oral presentations and scientific writing.
8. Collaborate effectively with
interdisciplinary teams, recognizing the value of diverse perspectives in
clinical research.
9. Prepare manuscripts for publication,
adhering to journal-specific guidelines and addressing peer reviewers' comments
professionally.
10. Demonstrate an understanding of the
entire clinical research process, from conceptualization to dissemination, and
the ability to apply these principles in their own research endeavors.
You have to attend 60% of the live sessions and fill out the survey to obtain the certificate.
1- Attending the live sessions of the two days.
2- fill out the survey.
