$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.