in clinical research managing our Trial Master File. The Trial Master File (TMF) is a collection of documentation that allows the... conduct of a clinical trial, and the integrity of the data produced, to be evaluated by regulatory bodies, such as the FDA...
within the Trial Master File (TMF); Gain hands-on training and exposure to the clinical trial start-up phase through our Site... required before the site begins to screen patients to participate in a clinical trial. The Regulatory Submissions Intern will provide...