Research Nurse Level 1 - Clinical Trials

Salary :

$90,235.6 - 103,724.4 yearly

Company : Peter Maccallum Cancer Centre

Job Type : Full Time

Melbourne

Number of Applicants

000+

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Job Description - Research Nurse Level 1 - 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.

YOUR ROLE IN THE FUTURE
Research Nurse Level 2 or Study Coordinator
• Ongoing, Full-Time Position (80 hours per fortnight, with one accrued day off per month)
• Location: Parkville, with flexible working arrangements (by agreement with manager)
• Salary:
o Research Nurse: $111,930 per annum
o Study Coordinator: $90,235.60 – $103,724.40 per annum
o Plus salary packaging, superannuation, and 5 weeks’ annual leave

About Us
The Parkville Cancer Clinical Trials Unit (PCCTU) coordinates clinical trials across three leading institutions within the Parkville medical precinct:
• Peter MacCallum Cancer Centre
• Royal Melbourne Hospital
• Royal Women’s Hospital

PCCTU is the largest oncology clinical trials unit in Australia, with a diverse and rapidly expanding clinical trials portfolio. Our strong focus on early-phase trials offers a dynamic and stimulating environment for experienced clinical research professionals.

About the Role
We are seeking an experienced Research Nurse (Level 2) or Study Coordinator with medical oncology and/or haematology clinical trials experience to join our multidisciplinary team. The successful candidate will demonstrate strong clinical trial experience within a hospital setting, excellent communication skills, and a collaborative approach to teamwork. Effective time management and the ability to manage multiple concurrent studies are essential.

For suitably experienced applicants, consideration may be given to appointment at a Senior Research Nurse or Senior Study Coordinator level. Full selection criteria are outlined in the Position Description.

Key Responsibilities
Working as part of a dedicated clinical trials team, the Research Nurse or Study Coordinator will be responsible for coordinating the delivery of direct and indirect patient care and associated data collection for multiple concurrent research studies. All activities will be conducted in accordance with:
• Therapeutic Goods Administration (TGA) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95)
• National Health and Medical Research Council (NHMRC) National Statement on Ethical Conduct in Research Involving Humans

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 trip 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 ADOs 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, 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.

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.
Hiring Manager: Nicole Marsh
Email: [email protected]
Phone: 03 855 98500

Applications Close: 11:59PM Thursday 19 February 2026

______________________________________________________________________________________________________

Position Summary

Under supervision, the Clinical Trials Research Nurse (level 1) will coordinate the delivery of direct and indirect care and associated data collection for concurrent research studies undertaken in the department, in accordance with the Therapeutic Goods Administration (TGA) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95) and the National Health and Medical Research Council (NHMRC) National Statement on Ethical Conduct in Research Involving Humans.

Enterprise Agreement

Nurses and Midwives (Victorian Public Sector) (Single Interest Employers) EnterpriseAgreement 2020-2024.

Classification or Salary Range

Research Nurse Level 1

Immunisation Risk Category

Immunisation Category A

Key Relationships

Internal

Research participants & their caregivers.

Multidisciplinary team members.

Clinical Trials Unit Staff.

All Peter Mac Clinical Research staff.

Clinical nurses in all relevant patient care areas - including SDS, OPD, ward nurses, diagnostic imaging nurses Principal Investigators, Co-investigators and associated clinical trial medical staff.

Departments implicated in clinical research external to CTU (pathology, diagnostic imaging, nuclear medicine, pharmacy, BaCT).

Health information services department.

Internal human research ethics committee (HREC).

External

Clinical Trial Sponsor representatives from pharmaceutical companies and collaborative groups.

Cancer Trials Australia.

Research nurses and data managers at other hospitals.

External laboratories and diagnostic imaging centres.

Professional bodies such as VCOG & COSA & ARCS.

Skills

Essential Requirements

Current registration with the Nurses Board of Victoria, with a minimum of 3 years post graduate oncology and/or haematology nursing experience, or relevant experience demonstrating the appropriate competencies and skills for the job and clinical setting.

Degree level education or other relevant further education.

Problem solving skills.

Personal integrity and discretion.

Demonstrated excellent team working skills with ability to work using own initiative.

Effective listening and interpersonal skills.

Time management skills and the ability to prioritize workload.

Desirable Requirements

Evidence of further education including post-graduate certification/diploma/continuous professional development specific to oncology/haematology and/ or clinical research.

Comprehensive IT skills.

Any previous research experience including working knowledge of Australian and International statutory and regulatory requirements including - TGA, FDA, EMEA

Certifications, Licenses & Registrations

AHPRA Registration

Key Accountabilities

Key Accountabilities

Demonstrated by / Key Performance Indicators

1. To effectively co-ordinate clinical research trials

Ensure conduct clinical research trials is in accordance with TGA ICH GCP and the NHMRC National Statement on Ethical Conduct in Research Involving Humans.

Practice at all times within current appropriate state and federal regulations and hospital policy.

Able to make appropriate clinical and professional autonomous decisions as appropriate to their current level of experience & seek clarification from senior colleagues where necessary.

Within their scope and level of competency, provide advice on the clinical aspects of a trial protocol to the Investigators & multidisciplinary team that is in accordance with TGA ICH GCP and the NHMRC National Statement on Ethical Conduct in Research involving Humans and in line with hospital policies and best clinical practice.

With supervision, provide advice on the regulatory and co-ordination aspects of a trial protocol to the Investigators & multidisciplinary team that is in accordance with ICH GCP and the NHMRC National Statement .

Work within the regulatory guidelines of the NHMRC Statement on Ethical Conduct in Research Involving Humans, unit operating procedures & hospital policy.

Maintain a flexible approach to working hours in order to meet the requirements of research protocols and subject recruitment.

Liaise with all involved groups/departments to ensure all biological samples are collected, processed, stored and shipped as per the clinical trial protocol requirements.

Participate in clinical trial monitoring/auditing internally and externally as required in order to meet the regulatory and scientific requirements.

Develop an effective working relationship with pharmaceutical company representatives (CRAs) during monitoring of clinical trial data, internal company audits and external reviews.

2. To undertake and participate in professional development and education

Undertake ICH GCP training, and PCCTU departmental mandated education modules and within the specified timelines fulfil the competencies listed in the PCCTU Clinical research nurse competency framework.

Participate in the teaching of nursing & medical staff and other members of the multidisciplinary team in regard to clinical research and associated guidelines & regulations in conjunction with senior colleagues.

Demonstrates a commitment to personal continuing professional development and participate in performance review/appraisal.

Undertakes additional training in order to acquire the knowledge and skills needed to implement new study protocols from a variety of clinical specialties, including neoplastic agent administration competency if this has not already been undertaken.

Key Accountabilities (Contd..)

3. Ensure quality data and patient safety at all times

Gain expertise to ensure interests of patients on clinical trials are met and protocol requirements are followed.

Maintain effective communication processes with patients and carers, investigators, and other members of the multidisciplinary team to ensure information is appropriately shared.

Always involve patients and their carers in decisions related to their care.

Work within the standards of care in the defined clinical trial protocols, SOPs and practice guidelines of the clinical trials unit, hospital policies & procedures to ensure adherence to and delivery of, a high quality service and seek guidance from senior colleagues as required.

Provide clinical care as required within their scope of practice and level of competency, including the administration of chemotherapy and other neoplastic agents if so trained.

Using existing clinical skills and expertise, contribute to the development of policies and procedures within the clinical trial unit & organisation to ensure that clinical practice within the trials unit is underpinned by current best practice.

Ensure that studies are undertaken in accordance with the terms approved by the institutional ethics committee and TGA. ICH GCP and the NHMRC National Statement on Ethical Conduct in Research Involving Humans.  Develop a knowledge of ICH GCP and the NHMRC National Statement on Ethical Conduct in Research Involing Humans and seek guidance from senior colleagues as required.

Develop a knowledge of each designated clinical trial protocol including procedures and documentation to ensure the safe and accurate conduct and recording of the study and seek guidance from senior colleagues as required.

Use practice guidelines and study specific documentation to ensure that data is recorded accurately and in accordance with regulatoryand privacy requirements.

Develop the ability to screen/register only appropriate patients for clinical trials as per clinical trial eligibility criteria. Follow patients as per protocol and, where necessary, facilitate participant withdrawal from a study in order to ensure the patients best care and the effective achievement of the study aims.

Ensure informed consent is obtained according to standard hospital practice, ICH GCP and the NHMRC National Statement on Ethical Conduct in Research Involving Humans and be actively involved in the ongoing informed consent process.

4. To function as an integral member of the clinical research team

Participates in appropriate quality activities.

Participates in unit meetings.

Takes responsibility for ensuring trial patients are seen by members of the delegated trial teams for trial visits. Take responsibility for ensuring protocol requirements are carried out in the absence of the trial co-ordinator/research nurse, seeking guidance from senior staff as required.

______________________________________________________________________________________________________

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.

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