• Patient screening and selection for first-in-class Transcatheter Mitral Valve Replacement (TMVR) clinical studies • Assist in developing materials to enable patient selection for TMVR studies based on complex analyses of medical imaging data, as well as other materials (reports summarizing findings, preparation of summaries etc ,) to support trial enrollments. • Independently owning the screening process end-to-end from image acquisition to final decision for inclusion/exclusion by an independent subject eligibility committee (SEC). • Interfacing and collaborating with physician investigators, directing, and training them to ensure that the right types of subjects are screened for the trial. • Proactively and critically examining ways to enhance overall clinical trial performance. • Providing ongoing feedback concerning all aspects of study screening experience for the purpose of developing and implementing strategies that will contribute to organizational and corporate goals and objectives. • Collaborating with the internal core clinical study team and clinical sites to share best practices and develop capabilities to optimize trial participation and contribution. • Complying with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. • Assisting with design, development, and monitoring of clinical evaluation projects.