As a Clinical Research Associate II, you will monitor clinical studies at investigative sites, ensuring they're conducted and reported per protocol. You'll coordinate activities, identify investigators, and help prepare regulatory submissions with an impeccable eye for detail. You will identify risks and take responsibility for the quality of your work.
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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 all activities to set up and monitor a study. You will identify investigators and help prepare regulatory submissions.