Our Clinical Research Associate (CRA) training offers an in-depth exploration of the clinical trial process, from initiation through to closeout. Developed by industry experts with extensive clinical trial and global monitoring experience, this course provides a solid foundation in Good Clinical Practice (GCP), Good Documentation Practice (GDP), and essential clinical trial documentation.
Key Learning Outcomes:
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Clinical Trial Lifecycle: Gain proficiency in managing clinical trials from study start-up to closeout, including protocol development, site selection, and monitoring.
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Regulatory Compliance: Understand and apply GCP and GDP standards to ensure adherence to regulatory requirements and maintain data integrity.
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Monitoring Visits: Learn to perform effective monitoring visits, ensuring compliance with trial protocols and regulatory guidelines.
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Documentation and Reporting: Master the creation and maintenance of essential clinical trial documentation, ensuring compliance with regulatory standards.
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Career Advancement: Upon successful completion, receive a certification recognized by sponsors, Contract Research Organizations (CROs), and regulatory bodies, enhancing career prospects in clinical research.
Who Should Enroll:
This course is ideal for professionals in the pharmaceutical, biotechnology, and clinical research sectors, including:
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Clinical Research Associates
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Clinical Trial Associates
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Clinical Research Coordinators
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Regulatory Affairs Specialists
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Quality Assurance and Compliance Officers
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Medical Affairs Professionals
Download Course Summary Leaflet
Click the link above to explore the complete course content in our PDF leaflet.
