Discover Vanderbilt University Medical Center : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world. It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged. Vanderbilt Health is committed to an environment where everyone has the chance to thrive and where your uniqueness is sought and celebrated. It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday. Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research. Organization: Pediatric Genetics Job Summary: Join a supportive, growing, multidisciplinary program caring for children and adults with heritable connective tissue disorders (HCTDs); including Ehlers–Danlos syndromes (HEDS/EDS subtypes), Marfan syndrome, Loeys–Dietz syndrome, arterial tortuosity, and related hypermobility and aortopathy conditions. You’ll be a billing provider for new and follow-up patients, own longitudinal care plans, and coordinate surveillance and supportive management across specialties. . Division Summary: The Division of Medical Genetics & Genomic Medicine in the Department of Pediatrics at Vanderbilt University Medical Center (VUMC) is a well-established, nationally recognized program providing comprehensive genetic care to patients from Tennessee and six surrounding states. Our multidisciplinary team includes eight clinical/metabolic geneticists, one PhD scientist, nine genetic counselors, 3 genetic counseling assistants, five nurse practitioners, and two metabolic dietitians. We are supported by strong state partnerships and work closely with colleagues across pediatric and adult medicine to deliver both outpatient and inpatient consultations. The division is an NIH Undiagnosed Diseases Network clinical site and a NORD-designated Rare Disease Center of Excellence. We are active in precision medicine initiatives, including leadership roles in the All of Us Research Program and the eMERGE network, and we host an ACGME-accredited clinical genetics fellowship, a combined Pediatrics/Genetics training program, and an ACGC-accredited genetic counseling master’s program. Our environment offers rich opportunities for collaboration in clinical care, research, and teaching, including participation in a robust clinical trials program. We are committed to professional development and provide a supportive, collegial setting for all team members to thrive.
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees