SCHN - Staff Specialist - Genetic Metabolic Disorders Service (eCredential)
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- Specialist
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- REQ574176 Requisition #
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- 1 day ago Post Date
Sydney Children's Hospitals Network is the largest paediatric health care entity in Australia. We care for thousands of children each year in our hospitals and in their homes — with one purpose in mind — to help young people live their healthiest lives.
Position Classification: Staff Specialist
Hours Per Week: 32
Requisition ID: REQ574176
The Western Sydney Genetics Program (WSGP), SCHN provides a comprehensive and integrated medical genetics service comprising the following departments:
- Clinical Genetics
- Genetic Metabolic Diseases Service
- NSW Biochemical Genetics Service
- Sydney Genome Diagnostics (Cytogenetic and Molecular Genetics)
- NSW Newborn Screening Program
- Academic Department of Medical Genetics
This comprehensive genetic diagnosis and counselling service is provided to clients of the Western Sydney
area and beyond, in addition to Statewide clinical services for Huntington disease, neurofibromatosis,
connective tissue dysplasia, phenylketonuria and other inborn errors of metabolism.
Statewide laboratory services are provided for newborn screening and biochemical genetics.
The Clinical Genetics Department and Genetic Metabolic Diseases Service in conjunction with other departments of the Hospital, provide joint management clinics for patients with limb deficiencies, connective tissue disorders, neuromuscular disorders and Rett syndrome.
In addition, outreach clinical services are provided to the greater Western NSW and Hunter New England health regions. This service provides an internationally recognised metabolic and screening service to the State of NSW, and
has been instrumental in developing new and important initiatives.
The position of Staff Specialist, Genetic Metabolic Disorders Service will ensure that:
- Clinical services are focused on delivering excellent clinical care to children and their supporting families
- Research and teaching is undertaken and focused on the area of Genetic Metabolic Disorders
The position will provide appropriate care to inpatients and outpatients as part of the Genetic Metabolic Disorders Service across the Sydney Children's Hospitals Network (SCHN).
The position will provide clinical support to the NSW Biochemical Genetics and Newborn Screening Services.
SCHN is an Equal Opportunity Employer that values diversity - we acknowledge the vibrancy that a diverse workforce brings to enhance both our workplace culture and our service delivery to children, young people and their families and carers. We encourage all suitably qualified applicants to apply. If you identify as an Indigenous Australian or as a person with a disability, please contact us if you would like some more information about our recruitment process.
Aboriginal and Torres Strait Islander people are encouraged to apply. We recognise the value of Aboriginal staff providing health care to Aboriginal children and families that access the services we provide at the Sydney Children’s Hospitals Network. Aboriginal job applicants are encouraged to visit the NSW Health Aboriginal Recruitment tool, Stepping Up to assist in preparing your application.
SCHN is committed to maintaining a child safe culture that upholds the rights of children and young people. We strive to ensure children and young people feel safe, supported, and are included in their care. Existing staff of SCHN and those seeking employment are required to prioritise the safety, wellbeing and best interests of children and young people in their care and take action to keep them safe from harm and abuse. Please click here for more information.
The preferred applicant may be considered for the award of a conjoint academic title (levels A to D) in the Faculty of Medicine and Health at the University of Sydney at a level commensurate with his/her qualifications and experience. The award of the academic title will also confer membership upon the appointee of the University Department of Paediatrics and Child Health. The academic title will be held for the duration of The Children's Hospital at Westmead appointment. No remuneration is attached to the University appointment. The appointee will be responsible to the University for academic matters and to The Children's Hospital at Westmead for clinical matters.
- Eligible for Specialist registration with the Medical Board of Australia (Australian Health Practitioner Regulation Agency - AHPRA)
- Fellowship of the Royal Australasian College of Physicians (Division of Paediatrics or Clinical Genetics or other relevant subspecialty) and/or other specialist recognition as provided for in the Staff Specialist (State) Award .
- Demonstrated recent clinical experience in Genetic Metabolic Disorders including the management of children, adolescents, and/or adults with inborn errors of metabolism
- Demonstrated ability to work effectively as part of a multidisciplinary team and provide leadership of a team and promoting a culture of continuous improvement
- Demonstrated effective clinical communication through the use of information technology and written, verbal and interpersonal skills
- Demonstrated commitment to teaching, continuing education, research and quality improvement
- Availability to participate in on call roster and to respond on site (both CHW and SCH) within a reasonable time.
Need more information?
1) Click here for the Position Description
2) Find out more about applying for this position
For role related queries or questions contact Julie Curtin on julie.curtin@health.nsw.gov.au
For technical support please contact the customer service team on 1300 679 367 and select option 3.
Applications Close: Wednesday, 21 May 2025
APPLY VIA eCredential NOW: CLICK HERE
Note: NSW Health does not require or accept the 'fit2work badge' offered as an option in eCredential. Please do not apply
or pay for a fit2work badge when applying for this position.
For assistance with eCredential please email SCHN-SMO@health.nsw.gov.au
