Clinical Research Associate II/Senior Clinical Research Associate

As a Clinical Research Associate, you will monitor and own the progress of clinical studies at investigative sites ensuring that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study, such as identifying investigators and helping prepare regulatory submissions. You will work with approximately 2-3 protocols on average and support Project Managers with trials that are larger in scope. You will interact directly with clients, initiate payments, and participate in proposal activities.