Medical Scientist – Clinical Trials Genome Analyst

Req ID: 7663

Date: 2 Aug 2026

Site: VCCC (Parkville)

Location:

MELBOURNE, VIC, AU, 3000

Company: Peter MacCallum Cancer Centre

Unit: Pathology Clinical Trials

Division: Business Ventures

Department: Pathology Operations

Enterprise Agreement: Medical Scientists, Pharmacists and Psychologists

Pathology Clinical Trials

Medical Scientist Gd2 – Clinical Trials Genome Analyst

Full time, ongoing role
Parkville location with flexible, hybrid working
Annual salary range between $94,479 - $106,907 + salary packaging + 12% super + 5 weeks annual leave

The Peter MacCallum Cancer Centre (Peter Mac) is a Victorian public health service and a world-leading comprehensive cancer centre, dedicated to excellence across all spheres of clinical care, research and education. We are home to the largest cancer research enterprise in Australia and provide treatment to around 40,000 people with cancer each year. Welcoming staff from diverse backgrounds and experiences is integral to fostering innovation and compassion and delivering the best possible cancer care for our patients.

About the team

Nexomics is a dedicated clinical trial division within the Peter MaCallum Cancer Centre. We deliver specialised clinical trial testing for internal stakeholders such as PCCTU and Research teams, under NATA ISO15189 and ISO17025 accreditation. In addition, Nexomics provides central lab services for clinical trials for commercial sponsors, CROs and biopharma companies globally.

About the role

This is a medical scientist role which is responsible for analysis and reporting clinical tests based on genetic and genomic assays.

Primarily this role will assist the clinical trial team in providing molecular pathology services that meet clinical trial requirements including TAT.

A regular day will see you:

Interprets and reports clinically significant results within the required TAT.
Assignment of pathogenicity to variants generated from sequence data.
Complete minimum of 5 cases per day.
Preparation and participation at various meetings including work planning and MDT.

About you

We are seeking a candidate who thrives in a fast-paced, dynamic environment, communicates effectively with both colleagues and external clients, and demonstrates the ability to manage and prioritise multiple tasks with confidence and efficiency.

You’ll bring with you:

Minimum qualification Bachelor of Science or equivalent with specific training and/or experience in human molecular genetics or diagnostics.
Minimum 3 years of experience in diagnostic pathology with specific experience in molecular pathology.
Minimum 1 year of experience and competency in analysis and reporting of NGS based diagnostic testing.
Minimum 1 year of experience in curation and interpretation of gene variance in cancer (preferably somatic variant curation and reporting).

Our benefits

We offer a range of benefits which support our people both personally and professionally, including:

Up to $11,660 in salary packaging to increase your take home pay
Discounted health insurance and eye care
A comprehensive health and wellbeing program
Public transport options at our doorstep and end of journey facilities for cyclists
Onsite eateries and coffee shops and inviting rooftop garden spaces
Pathways for professional development and new career opportunities
Five weeks annual leave, 17.5% leave loading, monthly ADO’s and purchased leave options
Flexible, hybrid working arrangements

Inclusion and belonging

Peter Mac celebrates, values and supports a diverse and inclusive environment which reflects our vibrant community. We encourage applications from anyone identifying as Aboriginal and/or Torres Strait Islander. We also welcome anyone who identifies as LGBTQIA+, linguistically, culturally and/or gender diverse, people with disability, and people of any age to apply for our roles.

Join us!

If you feel this role is right for you we warmly invite you to apply, and encourage your early application. All appointments are made subject to a satisfactory police check, and may require a valid Working with Children Check. Many staff are required to be vaccinated against, or demonstrate immunity to, COVID-19, influenza, and a range of other diseases.

Should you need assistance or require any adjustments or accommodations to fully participate in the application or interview process, you are welcome to reach out to the contact person listed. We acknowledge that not all applicants will meet the full list of selection criteria outlined, and wherever possible we will consider applications where relevant experience can apply.

For a confidential discussion about this role, please contact

Mariam Mohd Fadzil, mariam.mohdfadzil@petermac.org.

Applications Close 11:49pm: Monday 17 August 2026

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Position Summary

To support the clinical trials unit called nexomics to provide the highest quality of molecular services to the patients of Peter MacCallum Cancer Centre and its external clients. Key duties and responsibilities include (but are not limited to):
• Work as part of a collaborative team to analyse and report clinical tests based on genetic and genomic assays as directed by Team Leader responsible for section.
• Develop and maintain competency in the use of internal secondary and tertiary analysis platforms and external third-party data sources relevant to effective performance of the role.
• Provide leadership and training in molecular pathology, genomics data curation and interpretation.
• Maintain knowledge of medical/scientific literature relevant to the laboratory's testing programme.
• Prepare for and attend intramural / extramural MDTs and internal Pathology meetings.
• Maintain and enhance expertise by attending and contributing to Departmental and Research Division meetings and seminars, and relevant national and international forums.
• Improve and streamline reporting workflows.
• Prepare and maintain standard operating procedures.
• Conduct continuous quality improvement and ensure maintenance of accreditation.

Enterprise Agreement

Medical Scientists, Pharmacists, and Psychologists

Classification or Salary Range

RY4–RY7

Immunisation Risk Category

Key Relationships

Internal	Clinical Trials Operations Manager Senior Scientific Officer (nexomics) Clinical Trial technical staff (nexomics) Principal Scientist of Molecular Pathology Lead Scientist in Molecular Diagnostic Development Anatomical Pathologists Director of Pathology Quality Officers Clinical Trial Coordinators/Administrators (nexomics) Business Development team (nexomics)
External	External clinicians and clients Liaison with Pharma companies in relation to Clinical Trials

Skills

Essential requirements

BSc or equivalent with specific training and / or experience in human molecular genetics / diagnostics.
Demonstrated experience in/with:
Diagnostic pathology with specific experience in molecular pathology.
Competency in the analysis and reporting of NGS based diagnostic testing.
Curation and interpretation of gene variants in cancer, properties of oncogenic drivers, and relevance to targeted therapy selection.
Understanding of the principles of variant curation, HGVS nomenclature and interpretation of genomic results in the somatic context.
Laboratory quality systems, ISO 15189 standards, and medical laboratory accreditation procedures.
Ability to work interactively as part of an effective clinical team
Professional approach to patient care, service confidentiality and provision of laboratory services.
Communicate cooperatively in a team including with peer and senior scientists, pathologists, genetic counsellors, clinical staff and researchers.
Present work, write protocols and maintain documentation.

Desirable requirements

Experience with one or more of: data analytics, bioinformatics, clinical trials
Postgraduate qualification (MSc, PhD)
Relevant Professional Society Membership or Fellowship e.g. HGSA, FFSc(RCPA)

Key Accountabilities

Key Accountabilities	Demonstrated by / Key Performance Indicators
1. The provision of molecular pathology services that meet clinical trial requirements including TAT	Recognises, interprets and reports all clinically significant results including concise and informative explanations and recommendations based on appropriate medical literature. Efficient assignment of pathogenicity to variants generated from sequence data. Demonstrates customer focused conduct where commitment to effectively meeting the needs of clinicians and patients in a helpful and professional manner is paramount Keeps patient information confidential. Preparation, participation and presenting at variant meetings and multidisciplinary tumour board meetings. Participation in process improvement activities in the laboratory 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. All documentation is completed including procedures, maintenance records and quality assurance procedures according to laboratory, NPAAC and ISO 15189 standards and protocols.
2. Uses the laboratory LIS for processing and testing of all samples and understands the clinical implications of laboratory results	Recognises requirements for appropriate identification and labelling of specimens and request forms. Contacts the appropriate senior staff when information is required or results cannot be reported according to laboratory protocol.
3. Quality Service Provision	Professionally advises within and/or outside the laboratory on relevant laboratory and clinical matters. Communication with clinical staff and external clients as appropriate. Liaises well with other staff members to ensure that all testing adheres to protocol. Ensure all incidents and protocol deviations are documented and closed within a timely manner in consultation with the quality team. Seeks the advice of the senior scientific staff to solve any scientific and technical problems in the laboratory.
4. Knowledge enhancement	Regular and active contribution of knowledge of the medical/scientific literature, as relevant to cancer diagnosis and therapy, to enhance the future care of our cancer patients.

Key Accountabilities (Contd..)

Key Accountabilities	Demonstrated by / Key Performance Indicators
5. Participation in the validation and implementation of new assays and software	Participates in the validation of new assays and software in a timely manner
6. Quality Assurance	Promptly reports procedural breakdowns, errors and incidents to their supervisor. Participates in educational activities including attendance at internal and external training courses, clinical and scientific meetings. Maintains and develops own specialised skills. Embraces skill extension, innovation and change. 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.
7. Works as part of a team	Communicates and cooperates with co-workers to ensure work is completed within appropriate timeframes. Willingness and flexibility to work across a range of shifts is required, over a 7-day roster; including early shifts, late shifts and weekend work. Supports a workplace culture that encourages change, learning, innovation and a team-based approach with a client-responsive and patient-oriented emphasis.
8. Ethical Conduct	Acts in accordance with institution ethical guidelines and those established by relevant bodies. Patient/clinical trial confidentiality and privacy is protected.
9. Follows appropriate policies and procedures	Ensures that all work practices are safe and conform to institution OH&S guidelines and standards Acts in accordance with the Australian Institute of Medical Scientists (AIMS) professional code of conduct. Compliance with NPAAC guidelines for nucleic acid testing.
10. Maintain safe working practices and a safe working environment	Implement measures designed to minimise accidents and injuries (in consultation with Senior Scientist and Principal Scientists 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.

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Peter Mac is a child safe organisation and has a commitment to child safety and wellbeing.

WHY WORK FOR PETER MAC

• Peter Mac offer a range of benefits which support our people both personally and professionally.

• Our staff benefits include award winning facilities, professional development and events, a health and wellbeing program, flexible work practices and policies and financial benefits such as salary packaging.

• We encourage applications from Aboriginal and Torres Strait Islander people, all members of the LGBTQI community and people with a disability.