Understanding Clinical Research: Behind the Statistics

Course Feature
  • Cost
    Free
  • Provider
    ThaiMOOC
  • Certificate
    Paid Certification
  • Language
    English
  • Start Date
    4th Sep, 2023
  • Learners
    No Information
  • Duration
    No Information
  • Instructor
    Dr Juan H Klopper
Next Course
2.0
0 Ratings
This course provides an introduction to understanding clinical research and the statistical analysis behind it. It is designed to help both working professionals and medical students gain greater confidence in interpreting research results. The course covers topics such as confidence intervals and p-values.
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Course Overview

❗The content presented here is sourced directly from ThaiMOOC platform. For comprehensive course details, including enrollment information, simply click on the 'Go to class' link on our website.

Updated in [March 20th, 2023]

Learners can learn the basics of clinical research and statistics, including common statistical concepts and terms, how to interpret and understand published literature, and how to conduct their own research. They will also gain an understanding of the importance of clinical research and the impact it has on medical practice. Additionally, learners will be able to develop their skills in data analysis and interpretation, as well as gain an understanding of the ethical considerations of conducting clinical research. Finally, learners will be able to gain a certificate of completion and access financial aid if needed.

[Applications]
Those who have completed the course "Understanding Clinical Research: Behind the Statistics" can apply their knowledge to their own research or to properly understand the published literature. They can also use the certificate of completion to demonstrate their understanding of the course material. Additionally, those who need financial assistance can apply for Financial Aid to help cover the cost of the course.

[Career Paths]
1. Clinical Research Associate: Clinical Research Associates (CRAs) are responsible for the planning, implementation, and monitoring of clinical trials. They are responsible for ensuring that the trials are conducted in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP). CRAs are in high demand due to the increasing number of clinical trials being conducted. With the development of new technologies, CRAs are expected to have a greater understanding of the data generated from clinical trials and be able to interpret the results.

2. Clinical Data Manager: Clinical Data Managers (CDMs) are responsible for the collection, management, and analysis of clinical data. They are responsible for ensuring that the data is accurate and complete, and that it meets the requirements of the clinical trial protocol. CDMs are expected to have a strong understanding of the data generated from clinical trials and be able to interpret the results. With the development of new technologies, CDMs are expected to have a greater understanding of the data generated from clinical trials and be able to interpret the results.

3. Clinical Research Coordinator: Clinical Research Coordinators (CRCs) are responsible for the coordination of clinical trials. They are responsible for ensuring that the trials are conducted in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP). CRCs are expected to have a strong understanding of the data generated from clinical trials and be able to interpret the results. With the development of new technologies, CRCs are expected to have a greater understanding of the data generated from clinical trials and be able to interpret the results.

4. Clinical Trial Statistician: Clinical Trial Statisticians (CTSs) are responsible for the design, analysis, and interpretation of clinical trials. They are responsible for ensuring that the trials are conducted in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP). CTSs are expected to have a strong understanding of the data generated from clinical trials and be able to interpret the results. With the development of new technologies, CTSs are expected to have a greater understanding of the data generated from clinical trials and be able to interpret the results.

[Education Paths]
1. Master of Science in Clinical Research: This degree program provides students with the skills and knowledge to design, conduct, and analyze clinical research. It covers topics such as biostatistics, epidemiology, clinical trial design, and regulatory affairs. This degree is becoming increasingly popular as the demand for clinical research professionals grows.

2. Master of Public Health: This degree program focuses on the health of populations and communities. It covers topics such as health policy, health promotion, and health services administration. This degree is becoming increasingly popular as the need for public health professionals grows.

3. Doctor of Philosophy in Clinical Research: This degree program provides students with the skills and knowledge to design, conduct, and analyze clinical research. It covers topics such as biostatistics, epidemiology, clinical trial design, and regulatory affairs. This degree is becoming increasingly popular as the demand for clinical research professionals grows.

4. Doctor of Public Health: This degree program focuses on the health of populations and communities. It covers topics such as health policy, health promotion, and health services administration. This degree is becoming increasingly popular as the need for public health professionals grows.

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Pros & Cons
  • Comprehensive introduction to clinical research and medical statistics.
  • Clear explanation and comprehensive case study.
  • Understands the pros and cons of each test.
  • Needs more supplementary sources.
  • Lecturer only reads the script.
  • Not enough deep explanation of some issues.
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