Children's Hospital of Michigan has been a cornerstone of pediatric care since 1886 the first and largest children's hospital in the state, and consistently recognized as one of America's best by U.S. News & World Report. The Division of Genetic, Genomic, and Metabolic Disorders is one of Michigan's designated coordinating and referral centers for suspected metabolic disorders in newborns, with nearly 20 years of service behind it. You'll step into a well-resourced, academically engaged division with the latitude to shape your clinical, research, and leadership trajectory. This is a rare opportunity to grow a specialty program at an institution with the infrastructure, reputation, and mission to support it.

Position Highlights

• Full-time Biochemical Geneticist opening within an established genetics division at a 228-bed academic children's hospital affiliated with Central Michigan University
• Primary clinical focus on inborn errors of m...