Consultant Clinical Geneticist

Responsibilities

• Conduct comprehensive clinical genetics consultations and assessments for patients with suspected or confirmed genetic disorders.

• Diagnose and manage a wide range of inherited, congenital, and genetic conditions affecting children and adults.

• Evaluate patients with developmental delays, intellectual disabilities, congenital abnormalities, and suspected genetic syndromes.

• Assess individuals and families with a history of hereditary diseases and genetic conditions.

• Interpret genetic investigations, including chromosomal analysis, chromosomal microarray, next-generation sequencing (NGS), whole-exome sequencing (WES), and other molecular genetic tests.

• Develop individualised diagnostic and management plans based on clinical findings, genetic testing results, and evidence-based guidelines.

• Provide genetic counselling to patients and families regarding diagnoses, inheritance patterns, recurrence risks, and reproductive options.

• Assess and manage hereditary cancer syndromes in collaboration with oncology specialists, where applicable.

• Evaluate patients with rare genetic diseases and coordinate appropriate diagnostic investigations.

• Provide guidance on prenatal and preconception genetic testing, carrier screening, and reproductive genetic risks.

• Collaborate with pediatricians, neurologists, obstetricians, oncologists, laboratory geneticists, and other specialists.

• Participate in multidisciplinary meetings to discuss complex genetic cases and coordinate patient management.

• Provide long-term follow-up and appropriate referrals for patients with confirmed genetic conditions.

• Maintain accurate clinical documentation, genetic testing records, and patient medical histories.

• Ensure compliance with genetic testing regulations, patient confidentiality requirements, and ethical standards.

• Participate in clinical audits, research activities, and quality improvement initiatives.

• Stay up to date with advances in clinical genetics, genomic medicine, and molecular diagnostic technologies.

• Support teaching, training, and mentoring activities where required.

Qualifications

• Recognised specialist qualification in Clinical Genetics or Medical Genetics.

• Recognised Tier 1 specialist qualification, including ABMS, Canadian Royal College certification, UK CCT/CCST, European Board, or an equivalent recognised qualification.

• Minimum 2–5 years of post-specialisation experience in Clinical Genetics.

• Extensive experience diagnosing and managing inherited disorders, congenital abnormalities, and rare genetic diseases.

• Proven expertise in interpreting molecular genetic investigations, genomic sequencing results, and chromosomal studies.

• Significant experience providing genetic counselling and managing complex hereditary conditions.

• Experience working within a hospital, specialised genetics centre, or multidisciplinary clinical environment.

• Eligibility for Consultant-level licensing with DHA, DOH, or MOHAP.

Required Skills

• Strong clinical expertise in Clinical Genetics, Medical Genetics, and Genomic Medicine.

• Excellent diagnostic, analytical, and clinical decision-making skills.

• Proficiency in interpreting genetic testing results, including molecular and cytogenetic investigations.

• Strong knowledge of hereditary disorders, genetic syndromes, and inheritance patterns.

• Excellent genetic counselling and patient communication skills.

• Ability to manage complex genetic cases and develop individualised care plans.

• Ability to collaborate effectively with multidisciplinary healthcare teams.

• Strong understanding of ethical considerations, informed consent, and confidentiality in genetic testing.

• Commitment to patient safety, evidence-based practice, and continuous professional development.

Compensation

An attractive tax-free package will be offered based on the candidate’s qualifications, clinical expertise, professional experience, and background.