Open Rank Physician Scientist for MPS

University of North Carolina - Chapel Hill; Elkins Hills (NC); On-site; USD 120,000 - 180,000; Full time

Job summary

The University of North Carolina at Chapel Hill is seeking a Physician Scientist for its Division of Genetics and Metabolism. This full-time position focuses on both translational research and clinical genetic activities. The successful candidate will lead clinical research studies, manage patients with metabolic disorders, and engage in teaching. A strong MD educational background is required, along with excellent teaching skills. This is an equal opportunity employer welcoming diverse applicants.

Qualifications

• MD with board certification or eligibility in Pediatrics and Clinical Genetics/Biochemical Genetics.
• Excellent teaching skills and the ability to work effectively in a multidisciplinary team.

Responsibilities

• Lead translational research in the Muenzer MPS Center, including principal investigator duties.
• Provide clinical genetic services, evaluating and managing patients with various disorders.
• Participate in inpatient call with Pediatric Genetics/Metabolism team.
• Engage in teaching and scholarly activities.
• Seek extramural funding to support research initiatives.

Skills

Excellent teaching skills

Ability to work effectively in a multidisciplinary team

Education

MD with board certification or eligibility in Pediatrics and Clinical Genetics/Biochemical Genetics

Job description

Position Summary

The Division of Genetics and Metabolism in the Department of Pediatrics at the University of North Carolina at Chapel Hill is seeking a Physician Scientist to join the Dr. Joseph Muenzer MPS Research and Treatment Center. This full‑time, fixed term position is an open‑rank, variable‑track and/or tenure/tenure‑track faculty appointment. The role will spend 80% of the effort on translational research at the Muenzer MPS Center and 20% on clinical genetic activities within the Division. The candidate will serve as the principal investigator for ongoing and new MPS clinical research studies, aid in the clinical management of MPS patients, and contribute to teaching and scholarly activities. Collaboration with an interdisciplinary team of physicians, advanced practice providers, research staff, and health professionals is a key element of the position.

Responsibilities

• Lead translational research in the Muenzer MPS Center, including principal investigator duties for current and prospective clinical trials.
• Provide clinical genetic services by evaluating and managing patients with congenital abnormalities, connective tissue disorders, skeletal dysplasias, neurodegenerative disorders, and metabolic disorders in outpatient and inpatient settings.
• Participate in inpatient call with the Pediatric Genetics/Metabolism team.
• Engage in teaching, scholarly activities, and quality improvement projects as appropriate.
• Seek extramural funding to support research initiatives and enhance program visibility.

Minimum Education and Experience Requirements

MD with board certification or eligibility in Pediatrics and Clinical Genetics/Biochemical Genetics.

Excellent teaching skills and demonstrated ability to work effectively as part of a multidisciplinary team.

Preferred Qualifications, Competencies, and Experience

Track record with longitudinal research projects and exposure to MPS patients.

Equal Opportunity Employer Statement

The University is an equal‑opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities.