Medical Biochemical Genetics Physician
About The Position
Children's Hospital of Michigan has been a cornerstone of pediatric care since 1886 — the first and largest children's hospitals 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.
Requirements
- MD or DO degree required
- Board eligible or board certified in Clinical or Medical Biochemical Genetics and Clinical Genetics
- Must be eligible to obtain licensure in the State of Michigan
Nice To Haves
- Board eligibility or certification in Pediatrics or Internal Medicine desirable
Responsibilities
- Primary clinical focus on inborn errors of metabolism and lysosomal storage disorders
- Additional responsibilities include inpatient genetics consultation coverage and teaching of medical students, genetic counseling students, and pediatric residents
Benefits
- Competitive compensation commensurate with experience
- Academic affiliation with Central Michigan University supporting research and teaching engagement
- Opportunity to assume leadership roles within the division
- Support from a robust multidisciplinary team allowing strong focus on complex clinical cases
- Malpractice insurance provided
- Health, dental, and life insurance
- 401(k) with employer matching
- Deferred compensation program
- Relocation assistance
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree
