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.
Job listings
As a Clinical Research Associate, you will monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and regulations. You'll coordinate activities to set up and monitor a study, identify investigators, prepare regulatory submissions, and conduct pre-study and initiation visits. Your keen eye for detail and problem-solving skills will be crucial in identifying potential study risks and proposing solutions.
$91,500–$166,100
USD/year
Monitor and own the progress of clinical studies at investigative sites and ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate activities required to set up and monitor a study. Work with 2-3 protocols on average and support Project Managers with trials. Interact with clients, initiate payments, and participate in proposal activities.