Scientist Grade 2 - Nexomics

Req ID: 7501

Date: 26 Jun 2026

Site: VCCC (Parkville)

Location:

MELBOURNE, VIC, AU, 3000

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Company: Peter MacCallum Cancer Centre

Unit: Pathology Clinical Trials

Division: Business Ventures

Department: Pathology Operations

Enterprise Agreement: Medical Scientists, Pharmacists and Psychologists

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Pathology Clinical Trials

At Peter Mac we aim to continuously improve cancer care, research and education across all cancers and for all people affected by cancer: changing lives, breaking new ground. Everything we do is underpinned by our core values, Excellence, Compassion and Innovation. Welcoming people from a wide variety of different backgrounds and experiences is critical to fostering innovation, cultivating compassion, attracting and retaining top talent and providing the best possible cancer care for our patients.

Medical Scientist Grade 2 – Nexomics (Clinical Trials)

Full time (80hrs/fortnight), ongoing role

Parkville location, with multiple public transport options available

Salary range between $94,478 - $106,906 + salary packaging + 12% super + 5 weeks annual leave + monthly ADO

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 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

The purpose of this position is to prepare samples for analysis, provide testing and assist with method development within the molecular clinical trials team. This includes reviewing and report authorisation, participation in the validation of new molecular based tests and training of staff in new methodologies.

A regular day will see you:

Perform molecular testing using techniques such as NGS, ctDNA, PCR and Sanger sequencing.

Review and report molecular results.

Maintenance of laboratory supply and equipment.

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:

Bachelor of Applied Science (Medical Laboratory Scientist) or equivalent.

Minimum 3 years of experience as a medical scientist within the molecular area.

Minimum 3 years of experience in diagnostic and/or clinical trial testing.

Basic skills in Microsoft Office Suite and IT systems in healthcare setting

Demonstrate strong communication skills, 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 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

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

Hiring Manger: Mariam Mohd Fadzil

Email: [email protected].

Applications Close: 11:59pm Wednesday 9 July 2026

Position Summary

The purpose of this position is to prepare samples for analysis, provide testing and assist with method development within the molecular clinical trials team. This includes reviewing and report authorisation, participation in the validation of new molecular based tests and training of staff in new methodologies.

Enterprise Agreement

Medical Scientists, Pharmacists and Psychologists (Victorian Public Sector) (Single Interest Employers) Enterprise Agreement 2021-2025

Classification or Salary Range

RY4 – RY7

Immunisation Risk Category

Immunisation Category A

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,etc

Clinical Trial Coordinators/Administrators

Business Development team (Nexomics)

External External clinicians and clients

Liaison with Pharma companies in relation to Clinical Trials

Education

Bachelor of Applied Science in Medical Laboratory Science

Skills

Proven experience as a medical scientist within the molecular area

Experience in diagnostic and/or clinical trial testing.

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.

Key Accountabilities

1. Provision of molecular assays in the clinical trial environment •Providing molecular testing in the area of molecular pathology by use of various techniques NGS, ctDNA, PCR. Sanger sequencing, etc.

• Participates in review and reporting of molecular results.
• Smooth and efficient operation of daily workflow, including specimen receipt, tracking, test performance and reporting as required for the laboratory.
• Provides lab management duties for molecular clinical trials on a daily basis.
• Preparation of standard operating procedures and training of staff in clinical trial assays as required.
• Participate in the validation of new clinical trial assays including preparation of validation protocols and report (as required)
• Preparation of pre-trial documentation required for study implementation eg. Analytical plans, worksheets, etc.
• Participation in process improvement processes for the laboratory.
• Demonstrates an understanding of customer service for internal and external clients and is committed to effectively accommodating their requirements in a helpful and professional manner.
• Ensure turn-around-times are met.
• Development and application of methods and technologies.
• Successful and comprehensive QAP participation in local and international programmes.
• Liaises with pathologists and pathology staff to ensure a high quality clinical trials service.

2. Participation 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.
• Preparation of validation protocols and reports as guided by the Senior Scientist or delegate.
• Participates in the training of staff as indicating by the Senior Scientist or delegate.
• Maintains and develops own specialised skills including for professional development.

3. Maintenance of laboratory supply inventory and equipment •Maintenance of equipment, reagent supplies and control tissue stocks as directed

• 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.

Key Accountabilities (Contd..)

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 sample storage and filing.
• Maintains the study regulatory binders.
• 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.

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.

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 is required, over a 7 day roster, Including early shifts, late shifts and weekend work.

7. Ethical Conduct •Acts in accordance with institution ethical guidelines and those established by relevant bodies.

• Patient confidentiality and privacy is protected.

8. Work is performed safely •Ensures that all work practices are safe and conform to institution OH\&S guidelines and standards.

9. 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.