Children's Hospital of Michigan is seeking a full-time Biochemical Geneticist to join its established Division of Genetic, Genomic, and Metabolic Disorders. This role offers a unique opportunity to shape clinical, research, and leadership trajectories within a well-resourced, academically engaged division. The position is ideal for a physician looking to grow a specialty program at a renowned institution with strong infrastructure and a commitment to pediatric care.
Practice Info
- 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 metabolism and lysosomal storage disorders
- One of the few Lysosomal Storage Disease Clinics and Pediatric Enzyme Replacement Therapy programs in the state of Michigan
- Collaborative team includes a board-certified Clinical Geneticist, five advanced practice providers, six genetic counselors, two genetic counselor assistants, three registered nurses, and a dedicated dietician
- On-site Cytogenetics/Molecular Laboratory directed by board-certified laboratory geneticists
- Close collaboration with Wayne State University Genetic Counseling Graduate Program
Responsibilities
- Define the balance of clinical and research responsibilities based on interests and expertise
- Provide inpatient genetics consultation coverage
- Teach medical students, genetic counseling students, and pediatric residents
Compensation
- Competitive compensation commensurate with experience
Benefits
- Malpractice insurance provided
- Health, dental, and life insurance
- 401(k) with employer matching
- Deferred compensation program
- Relocation assistance
Requirements
- MD or DO degree required
- Board eligible or board certified in Clinical or Medical Biochemical Genetics and Clinical Genetics
- Board eligibility or certification in Pediatrics or Internal Medicine desirable
- Must be eligible to obtain licensure in the State of Michigan