The Senior Regional Clinical Research Associate (SRCRA) serves as the primary liaison to clinical trial sites participating in Corcept-sponsored studies. This role is responsible for managing site activities across all stages—qualification, initiation, monitoring, and close-out. The SRCRA ensures patient recruitment, enrollment, and overall site performance are aligned with GCP, ICH guidelines, and Corcept SOPs.
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.
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.
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.