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 (GDocP), and essential clinical trial documentation.
Key Learning Outcomes:
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Gain proficiency in managing clinical trials from study start-up to closeout, including protocol development, site selection, and monitoring.
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Understand and apply GCP and GDocP standards to ensure adherence to regulatory requirements and maintain data integrity.
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Learn to perform effective monitoring visits, ensuring compliance with trial protocols and regulatory guidelines.
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Master the creation and maintenance of essential clinical trial documentation, ensuring compliance with regulatory standards.
Who Should Enrol?
This course is ideal for professionals in the pharmaceutical, biotechnology, and clinical research sectors, including Clinical Research Associates, Clinical Trial Associates, Clinical Research Coordinators, Regulatory Affairs Specialists, Quality Assurance and Compliance Officers and Medical Affairs Professionals.
Download Course Summary Leaflet
Click the link above to explore the complete course content in our PDF leaflet.
If this course isn’t right for you, take a look at our other online clinical courses.
