Medical Scientist (Variant Curator, Diagnostic Genomics) - Pathology Services
Clayton, VIC, AU, 3168
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An exciting opportunity currently exists for an enthusiastic and experienced Medical Scientist (Variant Curator) Grade 2 to join our Diagnostic Genomics Laboratory. This is a full-time, ongoing position. Help shape the future of healthcare at Monash Health and embark on a rewarding career where your dedication makes a difference in people’s lives.
About the Monash Health Pathology Service
The Monash Health Pathology Service operates under the brand name Monash Pathology and is an integral part of Monash. It is the largest provider of Pathology services in the State of Victoria and currently operates 6 laboratories. The largest of these is located at the Monash Medical Centre, Clayton, with additional facilities being located at the Dandenong, Moorabbin, Casey, Victorian Heart Hospital and Wonthaggi Hospitals. There are currently 18 collection centres based within the hospital sites and community settings. Services are provided to the Public and Private sectors, and other laboratory services.
You will be joining Monash Health at an exciting time as we work in partnership with Alfred Health to be the premier shared public pathology service in Victoria. As a member of the pathology teams you will be helping shape the direction of this partnership.
About the Role
The Diagnostic Genomics Laboratory, Monash Pathology is made up of three different areas:
- The Cytogenetics Laboratory which processes a range of prenatal and postnatal specimens, using conventional and molecular diagnostic techniques. This includes DNA extraction, tissue culture, FISH, Microarray and Karyotyping.
- The Genetics and Molecular Pathology laboratory which provides a specialised genetic testing service for oncology, haematology as well as inherited diseases. Our genomics team currently offers DNA and RNA next generation sequencing (NGS) for targeted panels in solid tumour biology, haematology and cardiac. Additional NGS panels soon to be offered will include investigations into cancer predisposition disorders and WES for monogenic disorders.
- The Thalassaemia and Haemophilia Molecular laboratory’s role is to confirm the genetic basis for thalassaemia and other significant haemoglobinopathies, identify carrier status and perform prenatal testing for couples at risk of giving birth to children with severe disease. This laboratory also performs proband and carrier testing for Haemophilia A and Haemophilia B as well as prenatal testing.
The successful candidate will predominately assist the Diagnostic Genomics Laboratory to accurately identify and precisely classify and clinically report variants for Next Generation Sequencing (NGS) relating to cancer diagnosis (haematology and solid tumour), cancer predispostion disorders and inherited dieases. They will also be expected to contribute to Multidisciplinary Teams (MDTs) meetings, quality improvement, workflow optimisation, training and service development as well as documentation and the development of new assays and workflows.
About You
You have excellent written and verbal communication skills, with the ability and willingness to show initiative and application to the task at hand and to be a team player capable of interacting with a range of health professionals including oncologists, haematologists, pathologists, genetic counsellors, pathology laboratory and administrative staff. You will also have proven experience in a diagnostic laboratory setting with strong technical capabilities and commitment to quality outcomes. Prior experience with NGS variant curation and clinical reporting (targeted panels and/or WES) for oncology, haematology and/or inherited diseases is essential.
What You Need to Know
You should be able to demonstrate excellent communication skills as well as the ability to integrate into a small team environment. The successful applicant for this position will have at least a degree in Science or Biomedical Science (laboratory medicine or a recognised equivalent). Ideally the successful applicant will also have a relevant post-graduate degree.
Why you will love working with us
Ours is a connected team with strong shared values and an unwavering commitment to excellence. We are a highly skilled, collaborative, and welcoming team where the only limit in your career is you. Upon your appointment, we will provide you with
- A supportive and cohesive sub-team, working within a larger consumer relations team.
- Professional development courses, seminars and mentoring.
- Opportunities for you to use your experience in the role to inform and drive initiatives within the broader units and programs.
- Salary packaging.
- Onsite Gym options and ability to join Fitness Passport - your pass to an extensive choice of fitness facilities.
For a confidential discussion and to explore this opportunity further, please reach out to Dr. Suzanne Svobodova, Principal Scientist, Diagnostic Genomics Laboratory on 0475 741 954.
Position Description can be found here
Our Culture and Values
At Monash Health, our people are at the heart of everything we do. Our culture is inclusive, supportive and future-focused, underpinned by clear values and a commitment to continuous improvement.
Our teams play a critical role in bringing our new strategy to life, challenging traditional approaches, embracing innovation, and ensuring every appointment reflects our commitment to equity, transparency and excellence.
You’ll be encouraged to share ideas, contribute to improvement initiatives, and grow alongside experienced professionals who are passionate about what they do.
We are Full Hearted, Open Minded and All In, enabling excellent service delivery and a positive candidate and employee experience every time.
We recognise the value of equal employment opportunity. We are committed to patient safety, promoting fairness, equity and diversity in the workplace and to Child Safe Standards.
How to Apply:
Applications are accepted via the Monash Health online eHub system. For information including how to apply and probity check requirements, please click here for the ‘Application Guide’
Applications will be screened upon receipt and selection activity may commence prior to the closing date.
Applications close: 15 May, 2026