SCFHS Clinical Research Training Program-Intermediate
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About the ProgramThe Clinical Research Training program offers a foundational and practical introduction to the core areas of clinical research. It aims to build essential competencies in trial design, ethics, data management, scientific writing, statistical interpretation, and Real World Evidence (RWE) applications. The program blends theoretical frameworks with applied tools, equipping participants to operate within regulatory frameworks and real-world settings.
What You Will Learn• Introduction to Clinical Research
• Clinical Research Regulations and Ethical Guidelines
• Roles and Responsibilities in Research Teams
• Clinical Trial Planning and Execution
• Fundamentals of Real World Evidence (RWE)
• RWE Study Designs and Methodologies
• Scientific Documentation and Dissemination
• Statistical Analysis and Interpretation
• Data Management and Analytical Tools
• Project and Financial Oversight in Clinical Research
• Clinical Research Regulations and Ethical Guidelines
• Roles and Responsibilities in Research Teams
• Clinical Trial Planning and Execution
• Fundamentals of Real World Evidence (RWE)
• RWE Study Designs and Methodologies
• Scientific Documentation and Dissemination
• Statistical Analysis and Interpretation
• Data Management and Analytical Tools
• Project and Financial Oversight in Clinical Research
Skills AcquiredEthical conduct in clinical trials
Protocol and regulatory compliance
Clinical trial project planning
Data collection and analysis
Scientific writing and reporting
RWE study design development
Effective scientific communication
Budget and resource management
LevelThis program is intended for beginner to intermediate participants. It suits aspiring researchers, healthcare professionals, and others interested in gaining foundational and applied knowledge in clinical research aligned with international standards.