Clinical Research Associate

Job description

As a CRA you will have local responsibility for the delivery of the studies at allocated sites and you will be an active participant in the local study team(s). You will work in close collaboration with other CRAs and the Local Study Team/ Local Study Manager to ensure that study commitments are achieved in a timely and efficient manner. You will act as the main contact with the study site and have the responsibility for monitoring the study conduct to ensure proper delivery of the study. You will be responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with internal Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. The CRA will usually have these accountabilities: Contributes to the selection of potential investigators. Trains, supports and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles. Proves that site staff have completed and documented the required trainings appropriately, including ICH-GCP training,...