Monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all activities required to set up and monitor a study, such as identifying investigators and helping prepare regulatory submissions. The CRA will find quick and creative ways of overcoming difficulties.
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Monitor and own the progress of clinical studies at investigative sites ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate activities to set up and monitor a study and Senior CRAs handle clinical trials and support Project Managers with trials that are larger in scope.