Job Summary The central aspect of this role will be coordinating and facilitating clinical research, including but not limited to subject recruitment, regulatory submissions, data analysis/manuscript preparation, and maintaining databases for multi-site registries. Training related to research ethics, human subject protections, clinical study design, and data analytics and statistical methodology will be provided. The CRC will have opportunities to co-author medical journal submissions and will be encouraged to present results at regional and national meetings. We are a seeking responsible, motivated, and independent individual who will be completing or has completed an advanced degree in health-related areas and can commit a minimum of 2 gap years between college and medical/graduate school. This position may independently provide study coordination for simple and moderately complex clinical research studies. As a member of a coordination team, this position may help support a...