Clinical Trials Data Management and Quality Assurance
Master essential skills in clinical trials data collection, management, and quality assurance for maintaining data integrity and trial success.
Master essential skills in clinical trials data collection, management, and quality assurance for maintaining data integrity and trial success.
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.
4.8
(113 ratings)
10,492 already enrolled
Instructors:
Ann-Margret Ervin, PhD, MPH
English
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What you'll learn
Collect and manage clinical trials data effectively
Design robust data collection instruments
Implement database management systems
Conduct statistical performance monitoring
Ensure quality assurance in clinical trials
Skills you'll gain
This course includes:
5.8 Hours PreRecorded video
6 quizzes
Access on Mobile, Tablet, Desktop
FullTime access
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There are 6 modules in this course
This comprehensive course covers fundamental aspects of clinical trials data management and quality assurance. Students learn essential skills in designing data collection instruments, managing database systems, ensuring data integrity, and implementing quality control measures. The curriculum includes practical guidance on data assembly, cleaning, monitoring, and intervention management.
Data Collection Instruments
Module 1 · 1 Hours to complete
Data Management
Module 2 · 1 Hours to complete
Data Assembly and Distribution
Module 3 · 1 Hours to complete
Performance Monitoring
Module 4 · 29 Minutes to complete
Intervention Management
Module 5 · 1 Hours to complete
Quality Assurance
Module 6 · 49 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.
Ann-Margret Ervin, PhD, MPH
4.7 rating
86 Reviews
24,543 Students
3 Courses
Clinical Trials Expert and Associate Scientist at Johns Hopkins University
Dr. Ann-Margret Ervin is an Associate Scientist at Johns Hopkins University, with a focus on the design and conduct of randomized clinical trials, particularly in the field of ocular disease and visual impairment. Her research encompasses a wide range of topics, including age-related macular degeneration, cataracts, and diabetic retinopathy. Dr. Ervin serves as Co-Principal Investigator for several significant projects, including a multicenter observational study of Stargardt Disease and a clinical trial investigating the effects of lutein and zeaxanthin on ocular health. Additionally, she is engaged in research examining the ethical implications of federal regulations on institutional review boards (IRBs) and their impact on multicenter clinical trials.In her role at Johns Hopkins, Dr. Ervin also teaches courses on clinical trials management and quality assurance, contributing to the education of future public health professionals. Her extensive experience in clinical trial methodology and her commitment to improving research ethics make her a valuable asset to the field of epidemiology and public health.
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4.8 course rating
113 ratings
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