Scientist – Nexomics

Date: 20 Nov 2025

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

YOUR ROLE IN THE FUTURE
Scientist Grade 1

• Full Time Position with Monthly ADO
• Fixed Term until Jan 2027 (Parental Leave Cover)
• Parkville Location
• Salary: $63,674 - $91,785 (annual, full time equivalent) + salary packaging + 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 MacCallum Pathology Department. 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
To provide molecular testing in molecular haematology by use of various techniques including real-time PCR, HRM, fragment analysis and DNA sequencing including next generation sequencing.
This role would suit a candidate that enjoys working in a dynamic environment, can effectively communicate with their co-workers to ensure that all testing is completed within appropriate time frames and has the ability to manage and prioritise multiple tasks. We provide testing for a number of global clinical trials, so strong written and verbal communication skills are essential when liaising with our sponsors.

Victorian Department of Health has endorsed the initiative to restructure existing public pathology by bringing together laboratories into pathology networks operating under a lead health service.

Pathology services from the Royal Melbourne Hospital, Peter MacCallum Cancer Centre, the Royal Women’s Hospital and the Royal Children’s Hospital will transition to a single pathology service. This creates an exciting opportunity to strengthen the scope, scale and reach of pathology services across the Parkville precinct to benefit all Victorians.

This role will transition to the new pathology service which will be led by Melbourne Health

A regular day will see you:
• Perform molecular testing for clinical trial samples
• Support the development and validation of new molecular assays
• Perform equipment maintenance and general lab duties
• Liaise with internal and external stakeholders

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:
• BSc or equivalent in a relevant area of Genetics or Molecular Biology
• Minimum 1 year of experience as a Medical Scientist in molecular pathology or genetics laboratory
• Minimum 1 year of experience in a research laboratory or diagnositc and/or clinical trial testing
• Strong customer service skills and able to communicate professionally
Demonstrate strong organisational skills, attention to details and a team player

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
• 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 and monthly ADO’s

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 at mariam.mohdfadzil@petermac.org.

Application closing date: 11:59PM Sunday 7th December 2025

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Position Summary

This is a position that would suit scientists with experience in molecular pathology or clinical immunology/flow cytometry. The purpose of this position is to prepare samples for analysis, provide testing and assist with general laboratory assays as of part of the clinical trials portfolio.

Enterprise Agreement

Medical Scientists, Pharmacists, and Psychologists

Classification or Salary Range

Grade 1 (RX1-RX7)C

Immunisation Risk Category

Category A: Position involving direct patient contact, potential for exposure to blood, body fluid, human tissue specimens during course of a normal working day

Key Relationships

Internal	Clinical Trials Manager Senior Clinical Trial Scientists (nexomics) Clinical Trial technical staff (nexomics) Pathologists Quality Nominees Pathology staff within Molecular, AP, CSR, Admin, Haematology, Core lab etc. Clinical Trial Coordinators/Administrators Business Development team (Nexomics)
External	External clinicians and clients Liaison with Pharma companies in relation to Clinical Trials

Skills

Essential Requirements

Bachelor of Applied Science (medical laboratory science) or equivalent.
Experience in diagnostic and/or clinical trial testing.
Experience in one or more of the following disciplines; flow cytometry, ELISA, cryopreservation, cell separation, DNA/RNA extraction, PCR/qPCR, NGS Library Prep
Demonstrable abilities to work effectively within a team.
Works well under pressure and enjoys diverse portfolio of duties as required by the clinical trial portfolio.
Demonstrable abilities to multitask and effectively improve processes.
Attention to detail.
Ability to communicate effectively and promptly utilising electronic and other means.
Proven ability to work cooperatively with pathologists, clinicians, other senior scientists and researchers.

Desirable Requirements

Contribution and experience with validation of assays to NATA specifications.
Training in GCP and GDP.

Key Accountabilities

1.The provision clinical trial services, ensuring turn-around-times are met.	Providing sample processing services and laboratory testing in the area of molecular pathology or clinical immunology/flow cytometry by use of various techniques e.g. PBMC isolation, cryopreservation, NGS, ctDNA, PCR, Sanger sequencing, ELISA, flow cytometry. Processing of biological specimens. Smooth and efficient operation of daily workflow, including specimen receipt, tracking, test performance and reporting as required. Participation in process improvement processes for the laboratory. Demonstrates an understanding of customer service for internal and external customers and a commitment to effectively meeting their needs in a helpful and professional manner. Keeps patient information confidential. Ensure turn-around-times are met. All documentation is completed including procedures, maintenance records and quality assurance procedures according to laboratory, NATA ISO15189 and 17025, GCP, GLP and GDP standards.
2.Participate in the validation and implementation of new clinical trial assays	Participate in the validation of new clinical trial assays Preparation of standard operating procedures and training of staff in clinical trial assays as required.
3.Operates and maintains laboratory equipment as required	All equipment is operated and maintained in accordance with laboratory manuals and procedures. Ensures the maintenance records of laboratory equipment are kept according to laboratory protocols.
4.Uses the laboratory quality system for processing and testing of all samples and has a basic understanding of the clinical implications of laboratory results.	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 relevant client or other staff when additional information is required, or specimens cannot be processed according to the clinical trial protocol. Is familiar with the internal and external quality control activities within the laboratory and complies with the relevant QC protocols. Ensures that all clinical trial/study samples are processed as per the study and/or laboratory manual. Seeks the advice of the senior scientific staff to solve any scientific and technical problems in the laboratory.
5.Quality assurance	Validates new processes and equipment. Promptly reports procedural breakdowns, errors and incidents by means of the non-conformance reporting system. 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.

Key Accountabilities (Contd..)

6. 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 if required, over a 7 day roster, Including early shifts, late shifts and weekend work
7. Helps maintain external client base	Cooperates with and assists external clients. Participate in any audits, site qualification visits and monitoring visits as required
8. Ethical Conduct	Acts in accordance with institution ethical guidelines and those established by relevant bodies. Patient confidentiality and privacy is protected.
9. Work is performed safely	Ensures that all work practices are safe and conform to institution OH&S guidelines and standards
10.Professional approach to work	Acts in accordance with institution policies in all matters

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For further information about this opportunity, click Apply to be redirected to the Peter Mac Careers page where you can review the position profile. Alternatively, please contact us for a confidential discussion.

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.