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 necessary activities required to set up and monitor a study. Work with 2-3 protocols and support Project Managers with trials that are larger in scope, while interacting directly with clients.
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USD/year
Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all necessary activities required to set up and monitor a study. Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.