In this course, you’ll learn about the more advanced elements of managing clinical trials. From anticipating and planning for protocol events to conducting systematic reviews to synthesize evidence, you and your study team need the skills to implement best practices throughout the trial process. You’ll learn how to recognize and respond to problems and adverse events, comply with regulations, and participate in frameworks that promote transparency. You’ll also learn how systematic review and meta-analysis is used to synthesize evidence from multiple sources. Finally, you’ll learn how your research can benefit from the adoption and consistent use of standardized study documents.
This course is part of the Clinical Trials Operations Specialization
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About this Course
Learners should have some familiarity with basic scientific, statistical, and management concepts.
Could your company benefit from training employees on in-demand skills?
Try Coursera for BusinessWhat you will learn
Detect and respond to protocol events
Recognize and respond to misconduct
Safeguard participant safety and trial integrity
Develop and maintain study documents
Skills you will gain
- Ethics
- Reproducibility
- Meta-Analysis
- Compliance
- Evidence Synthesis
Learners should have some familiarity with basic scientific, statistical, and management concepts.
Could your company benefit from training employees on in-demand skills?
Try Coursera for BusinessOffered by
Syllabus - What you will learn from this course
Protocol Events
Regulatory Affairs and Trial Misconduct
Standardization, Transparency, and Research Reproducibility
Evidence Synthesis: Introduction to Systematic Reviews and Meta-Analysis
Reviews
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- 4 stars6.25%
- 1 star6.25%
TOP REVIEWS FROM CLINICAL TRIALS MANAGEMENT AND ADVANCED OPERATIONS
Interesting literature with great insight for procedure for compliance with regulatory agencies for clinical trial .
About the Clinical Trials Operations Specialization

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