Clinical Research Associate (CRA) training is essential for individuals interested in working within the pharmaceutical industry, particularly in managing and monitoring clinical trials. CRAs play a critical role in ensuring that clinical trials are conducted ethically, safely, and in compliance with regulatory standards.
The training agenda for Clinical Research Associates (CRAs) in the pharmaceutical industry typically covers a broad range of topics to ensure that CRAs are well-versed in the clinical trial process, regulatory requirements, and effective site management. Here is a general outline of the main agenda for CRA training 1. Introduction to Clinical Research and Drug Development 2. Regulatory Requirements 3. Clinical Trial Protocol 4. Investigational Product (IP) Management
