As a team or project wizard support staff and contacts in clinical research in the conduct of clinical trials, project management and administrative processes.
In this intensive seminar you will receive a brief overview of the phases of clinical development and post-approval. The legal principles and terminology and GCP requirements are clearly presented and are suitable for refreshing existing knowledge.
By the acquired background knowledge you are able to take over its own administrative tasks, such as compiling the documents for the preparation and initiation of a clinical trial, for example, test centers, authorities and ethics committees. You know the deadlines for and deadlines, monitor them accordingly in order to assist your academic manager and the study team specifically.