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The main function of a clinical research associate is to monitor clinical trials. A clinical research associate ensures compliance with the clinical protocol, checks clinical site activities, makes on site visits, reviews Case Report Forms and communicates with clinical research investigators. A clinical research associate is usually required to possess an academic degree in Life Sciences and needs to have a good knowledge of Good clinical practice and local regulations (e.g. in the United States, the code of federal regulations also known as 21 CFRs).
- International Conference on Harmonisation
- United States Food and Drug Administration
- Society of Clinical Research Associates (United States)
- Association of Clinical Research Professionals (United States and United Kingdom)
- Clinical Research Nurses Association (United Kingdom)
- The Belmont Report: Ethical Principles and Guidelines for Research Involving Human Subjects
- Certified Clinical Research Associate Program
- Institute of Clinical Research (United Kingdom)
Clinical Trials BookstoreEdit
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