Clinical Trials Analysis, Monitoring, and Presentation
Master clinical trial operations with focus on sample size calculation, monitoring, and results analysis. Perfect for healthcare professionals and researchers.
Master clinical trial operations with focus on sample size calculation, monitoring, and results analysis. Perfect for healthcare professionals and researchers.
This course cannot be purchased separately - to access the complete learning experience, graded assignments, and earn certificates, you'll need to enroll in the full Clinical Trials Operations Specialization program. You can audit this specific course for free to explore the content, which includes access to course materials and lectures. This allows you to learn at your own pace without any financial commitment.
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What you'll learn
Calculate appropriate sample sizes for clinical trials
Implement effective trial monitoring procedures
Analyze clinical trial results using statistical methods
Create comprehensive trial monitoring reports
Communicate trial results through professional publications
Skills you'll gain
This course includes:
4 Hours PreRecorded video
5 quizzes
Access on Mobile, Tablet, Desktop
FullTime access
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There are 5 modules in this course
This comprehensive course teaches advanced operational skills for successful clinical trial management. Students learn essential concepts including sample size calculation, statistical monitoring methods, and results reporting. The curriculum covers trial monitoring for safety and efficacy, data analysis techniques, and advanced topics like adaptive designs and Bayesian approaches. The course provides practical knowledge for analyzing, monitoring, and presenting clinical trial data effectively.
Clinical Trial Sample Size
Module 1 · 51 Minutes to complete
Trial Monitoring
Module 2 · 41 Minutes to complete
Reporting Results From Randomized Clinical Trials
Module 3 · 1 Hours to complete
Analyzing Trials
Module 4 · 42 Minutes to complete
Advanced Topics
Module 5 · 46 Minutes to complete
Fee Structure
Instructors
Associate Professor, Epidemiology
My primary interest is in the design, conduct, and analysis of multicenter clinical trials. Many of the trials we have completed are comparative effectiveness trials - head to head comparisons of competing treatment with patient-centered outcomes. Most of my experience has been in trials of treatments for eye disease and asthma.
Senior Scientist and Biostatistics Expert at Johns Hopkins University
Dr. Elizabeth A. Sugar is a Senior Scientist at Johns Hopkins University, where she specializes in biostatistics with a focus on the design and analysis of clinical trials and observational studies. Her research interests include developing innovative statistical methods for clinical trials, particularly in oncology, where she has contributed to numerous high-impact studies. Dr. Sugar teaches courses on clinical trials analysis, monitoring, and presentation, as well as the design and conduct of clinical trials, equipping students with essential skills for effective research in public health.With a strong academic background that includes a PhD in Statistics from the University of Washington, Dr. Sugar has been instrumental in advancing methodologies that enhance the reliability and validity of clinical research. Her extensive experience in both academic and practical applications of biostatistics positions her as a key figure in the field, dedicated to improving health outcomes through rigorous scientific inquiry.
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