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Bayside Health seeks a Clinical Research Ethics Associate to support the Malignant Haematology team with trial start-up and post-approval work at The Alfred. You will coordinate RCDs, quotes and declarations of support, and ensure meticulous archiving of trial documents.
The role emphasises high-level admin, clear communication with department heads and external stakeholders, and experience within cancer services or hospital settings.
Bayside Health is a public health service delivering high-quality care across every stage of life for close to 1.2 million people living in metropolitan Melbourne, the Mornington Peninsula, Koo Wee Rup, Bass Coast and Southern Gippsland. We have more than 15 main sites, including hospitals, centres and clinics that provide comprehensive care from welcoming newborns to supporting older people and a full range of services in between. More than 22,000 dedicated staff are focused on providing exceptional, equitable, and locally connected care through shared expertise, compassion, and a commitment to continuous growth. Education and training are central to staff development as we encourage all employees to strive and thrive. Bayside Health was formed following the merger of Alfred Health, Bass Coast Health, Gippsland Southern Health Service, Kooweerup Regional Health Service and Peninsula Health on 1 January 2026.
The Malignant Haematology and Stem Cell Transplantation Service and the Haemostasis / Thrombosis Unit, and the Haemophilia Centre, support haematology patients from the greater Melbourne area, and adult haemophilia patients from all of Victoria. The Clinical Research Unit ("CRU") oversees a range of clinical trials for these diverse patient groups from Phase 1, first-inhuman to Phase 3 randomised, controlled trials, testing newly developed drugs straight from the biotech companies to established drugs used in new regimens. A Collaborative Group called the Australasian Myeloma Research Consortium (AMaRC) is run from our unit. AMaRC promotes, facilitates and sponsors Investigator-initiated trials and collaborative laboratory research projects in myeloma, acting as Trial Centre supporting the participating sites in Australasia.
The Clinical Research Ethics Associate is responsible for supporting their immediate team with administrative tasks associated with clinical trial start-up and post-approval. This will predominantly include:
For enquiries regarding this position, please contact Louise Javier, Senior Clinical Trial Coordinator - l.javier@alfred.org.au
Applications close 11pm AEDT, Sunday 18th October 2026.
We embrace diversity and strive to have a workforce that reflects the communities we serve. We actively encourage applications from Aboriginal and Torres Strait Islander people, people with disability, and people of all genders, sexualities, and cultural backgrounds.
If you require adjustments to the recruitment and selection process, or require an alternative format to any of the application materials, please don’t hesitate to get in touch with the contact person listed on this ad.
In accordance with the Health Services Amendment (Mandatory Vaccination of Healthcare Workers) Act 2020, health care workers in Category A or B roles (as determined by the department’s risk ratings) are required to be vaccinated against influenza or hold an acceptable medical exemption.