Scientist Grade 2 – Molecular Pathology Analyst

Clinicians, genetic counsellors, researchers, and pathology scientists

Clinicians, external clients and institutions

• BSc or equivalent with specific training and / or experience in molecular diagnostics.
• Demonstrated experience in diagnostic pathology with specific experience in high throughput diagnostic molecular pathology.
• Demonstrated experience and competency in the analysis and reporting of both NGS based and non-NGS based diagnostic testing.
• Demonstrated experience and understanding of the principles of variant curation, HGVS nomenclature and interpretation of genomic results in relevant clinical context.
• Demonstrated experience with laboratory quality systems (Qpulse experience preferred).
• Demonstrated experience with preparing and maintaining NATA documentation.
• Recognised scientific training and competence relevant to the position including appropriate knowledge and experience in laboratory services, quality systems, information technology, analytical methods and techniques used.
• Interpersonal attributes necessary to work as part of an effective and clinically interactive team.
• Professional approach to patient care, service confidentiality and provision of pathology/testing services.
• Ability to communicate effectively.
• Demonstrated ability to meet the clinical expectations of client.
• Demonstrated ability to work and communicate cooperatively in a team including other scientists, senior scientists, pathologists, genetic counsellors, clinical staff and researchers.
• Demonstrated ability to present work, write protocols and maintain documentation

• Postgraduate qualification (MSc, PhD).
• Relevant Professional Society Membership and Fellowship (eg. HGSA, FFSc (RCPA)).
• Experience with one or more of: automated sequencing (Sanger & NGS), high resolution melting, genotyping, real-time PCR, digital PCR and bio-informatics.

• Demonstrated experience and competence to make independent analytical decisions in the performance and understanding of a wide range of diagnostic tests or procedures or of complex tests
• Demonstrated ability to critically assess and evaluate reporting products or workflows
• Mentoring and/or training of undergraduate and graduate scientific staff within laboratory protocols
• Efficient management of resources so that the laboratory’s clients are satisfied the service meets the clinical needs of their patients and test results / reports are issued with clinically acceptable turnaround times.
• Efficient assignment of pathogenicity to variants generated from sequence data.
• Validation and authorization of reports including signing out when delegated from Team Leader(s) or Principal Scientist for Molecular Pathology
• Smooth and efficient operation of reporting workflow including analysis and reporting as required.
• Minimal disruption to continuity of service delivery
• Demonstrates an understanding of customer service for internal and external customers and is committed to effectively meeting their needs in a helpful and professional manner.
• Keeps patient information confidential
• Monitors, and adheres to key performance indicators.
• All documentation is completed including procedures, maintenance records and quality assurance procedures according to laboratory, NATA ISO15189 standards and protocols.

• N/A

• Ensures the appropriate identification and labelling of specimens and request forms, processing of all specimens for assay or dispatch to other laboratories, data entry of all relevant patient and testing information.
• Contacts the requesting medical officer or other staff when additional information is required or specimens cannot be processed according to laboratory protocol.
• Is familiar with the internal and external quality control activities within the laboratory and complies with the relevant QC protocols.

• Demonstrated ability to provide professional advice within and/or outside the laboratory on appropriate scientific/clinical matters
• Communication with clinical staff and external clients as appropriate
• Liaises well with other staff members to ensure that all molecular pathology testing adheres to the relevant protocols.
• Seeks the advice of the senior scientific staff to solve any scientific and technical problems in the laboratory.

• Participates where appropriate in internal and external QA programs.
• Participates in educational activities including attendance at internal and external training courses, clinical and scientific meetings.
• Demonstrated commitment to further education and ongoing professional development, which may include attendance at scientific meetings and activities recognised through the Australian Institute of Medical Scientists or equivalent professional body
• Maintains and develops own specialised skills.
• Embraces skill extension, innovation and change.

• Communicates and cooperates with co-workers to ensure work is completed within appropriate timeframes.
• Supports a workplace culture that encourages change, learning, innovation and a team-based approach with a client-responsive and patient-oriented emphasis.

• Implement measures designed to minimise accidents and injuries (in consultation with Senior Scientists and Principal Scientist for Molecular Pathology)
• Ensure laboratory compliance with relevant OHS legislative and regulatory requirements.
• Ensure that all incidents and near misses are reported in the appropriate system and that these records are used for continuous safety improvements.
• Liaison with OHS representative.

• Acts in accordance with the Australian Institute of Medical Scientists (AIMS) professional code of conduct.
• Compliance with NPAAC guidelines for nucleic acid testing.