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Consultant Paediatric Metabolic Genetics - Al Ain

Job Summary
We are seeking a highly qualified and experienced Consultant Paediatric Metabolic Genetics Specialist to join a leading healthcare facility in Al Ain. The successful candidate will diagnose, manage, and provide long-term care for infants, children, and adolescents with inherited metabolic and genetic disorders while delivering evidence-based, patient-centered care in a multidisciplinary environment.
Key Responsibilities
  • Diagnose and manage inherited metabolic disorders and genetic conditions in pediatric patients.
  • Evaluate patients with suspected metabolic diseases, developmental delays, neuromuscular disorders, and rare genetic syndromes.
  • Interpret metabolic, biochemical, and genetic investigations including newborn screening results.
  • Develop individualized treatment and long-term management plans for patients with metabolic and genetic disorders.
  • Provide inpatient and outpatient consultations for pediatric metabolic genetics cases.
  • Collaborate with neonatologists, pediatric neurologists, dietitians, genetic counselors, laboratory specialists, and multidisciplinary healthcare teams.
  • Provide counseling and education to patients and families regarding diagnosis, treatment options, inheritance patterns, and long-term care.
  • Participate in newborn screening programs and metabolic emergency management.
  • Maintain accurate clinical documentation in compliance with DOH regulations and hospital policies.
  • Participate in research, clinical audits, teaching, and continuous medical education activities.
Qualifications & Requirements
  • MBBS or equivalent medical degree recognized by DOH Abu Dhabi.
  • Board Certification / Fellowship in Paediatric Metabolic Genetics, Clinical Genetics, or Metabolic Medicine.
  • Valid DOH Consultant License or Eligibility Letter in the relevant specialty.
  • Minimum 5–7 years of post-board consultant experience in pediatric metabolic genetics within a tertiary care or academic hospital.
  • Strong expertise in inherited metabolic disorders and pediatric genetic diseases.
  • Excellent communication, analytical, and multidisciplinary teamwork skills.
Preferred Skills
  • Experience in newborn screening and metabolic emergency protocols.
  • Exposure to rare disease programs and genomic medicine.
  • Research publications and academic experience are an advantage.
  • Ability to work in a multicultural healthcare environment.
Benefits
  • Competitive tax-free salary
  • Family benefits
  • Health insurance
  • Annual airfare allowance
  • Paid annual leave
  • CME and professional development support

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