Sr CRA (Level I) - FSP

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Sr CRA must have a minimum 3-5 years' experience as a monitor and can work independently and monitor all stages of a study, in different phases, and should have special therapeutic expertise (oncology). The Sr CRA can take on-board LST tasks and support the LST in coordination or document preparation as and when required but their main task is still independent and advanced monitoring. Ability to travel internationally as required. Valid driving license. Short role description The Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The SrCRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The SrCRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ 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. A SrCRA with longer tenure and experience may take on additional responsib