Course Content
Introduction to Clinical Research
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Overview of Clinical Research
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Role of the Clinical Research Coordinator (CRC)
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Ethical Considerations
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Overview of Clinical Trials
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Good Clinical Practice (GCP)
Regulatory Requirements and Compliance
Study Design and Protocol Development
Site Management and Coordination
Data Management and Documentation
Monitoring and Auditing
Clinical Trial Financial Management
Ethics and Legal Aspects of Clinical Research
Preparing for the CCRC Certification Exam
Post-Certification and Career Development
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