• Monitor and own the progress of clinical studies at investigative sites • 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 • Work with 2-3 protocols on average and support Project Managers with larger scope trials • Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations