Clinical data management (CDM) manages the data protocols for clinical trials, including establishing the right systems, processes, procedures, and training to extract meaningful results and comply with local and federal regulations around the world.
Clinical data management ensures that data collected throughout — and resulting from — a clinical trial is accurate, reliable, and compliant with regulatory standards. It protects the integrity of the trial and lays a foundation on which innovation can begin to take place.
Managing data that arises out of a clinical trial is a big job. The number of data points for just Phase III trials tripled to 3.6 million data points over the course of 10 years. Connecting the dots between all this information and setting up structures that enable researchers to turn them into insights and innovation is at the heart of clinical data management.
You’ll learn how to
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