Clinical Research Trials jobs in Melbourne VIC
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- Orygen, The National Centre of Excellence in Youth...Parkville VIC
- Salary packaging
- Transportation links
- Research governance - Ensure site activities align with Orygen's Research Governance Framework, helping streamline how research is conducted across Orygen-…
View similar jobs with this employerPeter MacCallum Cancer CentreParkville VIC- Annual leave
- Insurance services
- Salary packaging
- Post graduate qualifications in oncology, haematology and/or clinical trials research.
- To ensure that all clinical trials are managed according to the…
- FortreaMelbourne VIC
- Basic understanding of the clinical trial process.
- Assist with the administration of clinical research projects, recruiting investigators (if applicable),…
- Safer Care VictoriaMelbourne VIC
- The Manager, Research Strategy and Clinical Trials leads the delivery of key state‑supported research and clinical trials functions within Safer Care Victoria.
- Australian Catholic UniversityMelbourne VIC
- Salary packaging
- The Clinical Trials Project Coordinator will be responsible for key aspects of investigator-initiated trials including applying for human ethics, registration…
- St Vincent's Health AustraliaMelbourne VIC
- Salary packaging
- Database management and data capture (endoscopic / clinical).
- Assisting with the ongoing Clinical Trials and departmental research in the Gastroenterology…
- Department of HealthMelbourne City Centre VIC
- The Manager, Research Strategy and Clinical Trials leads the delivery of key state-supported research and clinical trials functions within Safer Care Victoria.
View similar jobs with this employerAustin HealthHeidelberg VIC 3084- Health insurance
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- Manage the care of patients participating in clinical trials, ensuring compliance with the trial protocol, reporting requirements and ethical guidelines.
- The Royal Women's HospitalParkville VIC
- Annual leave
- Salary packaging
- Previous research experience including the conduct of trials.
- Work collaboratively and supportively with members of the clinical and broader research team.
- The Royal Women's HospitalParkville VIC
- Annual leave
- Salary packaging
- Previous research experience including the conduct of trials.
- Work collaboratively and supportively with members of the clinical and broader research team.
- Peter MacCallum Cancer CentreParkville VIC
- Annual leave
- Insurance services
- Salary packaging
- Handling of clinical trial and referred specimens • All clinical trial and referred specimens are handled, processed and dispatched in accordance with protocols…
- St Vincent's Health AustraliaMelbourne VIC
- Salary packaging
- Excellent benefits including salary packaging.
- Full time fixed term until 30/01/2027.
- You will work as part of the Biochemistry team to produce accurate, high…
- University of MelbourneParkville VIC 3010
- Parental leave
- Health insurance
- Employee assistance program
- Salary packaging
- Join us to advance evidence-based treatments for childhood conduct disorder and build your clinical research career.
- Monash UniversitySt Kilda Road VIC
- Working across a diverse range of activities, you will help coordinate clinical trial operations, streamline administrative processes and provide trusted…
View similar jobs with this employerAustin HealthMelbourne Northern Suburbs VIC- Health insurance
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- CREDO has a strong and successful history in conducting numerous clinical trials in metabolic disorders with most trials focusing on diabetes and obesity.
- Victoria UniversityFootscray VIC
- Undertake quality academic research, typically in collaboration with research students and/or research staff.
- Assist with supervision of research undergraduate/…
- View all Victoria University jobs - Footscray jobs - Research Fellow jobs in Footscray VIC
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Job Post Details
Clinical Research Associate - job post
Parkville VIC•Hybrid work
$125,000 - $135,000 a year - Full-time, Contract
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Job details
Pay
- $125,000 - $135,000 a year
Job type
- Contract
- Full-time
Location
Parkville VIC•Hybrid work
Benefits
Pulled from the full job description
- Salary packaging
- Transportation links
Full job description
-
Research Parkville, VIC Full time, contract
17/7/2026
- Parkville/hybrid opportunity | Close to public transport
- Full or part time 2-year contract | 0.8-1.0 considered
- Supportive on the job development | Join a passionate team
About Orygen
Orygen is Australia’s Centre of Excellence in Youth Mental Health and the largest translational research organisation dedicated to youth mental health in the world.
For over 30 years, Orygen has led groundbreaking early intervention and developed evidence-based models of care to improve the mental health outcomes of young people aged 12-25.
About the job
The Clinical Research Associate will contribute to and support the regulatory compliance of Orygen research projects to ensure Good Clinical Practice compliance as well as assist in the development and maintenance of the Quality Management System (QMS). A key aspect of this role is to ensure all research projects across Orygen are conducted in accordance with best practice.
Reporting to the Head of Sponsor Operations you will:
The following criteria must be met for consideration for this position:
If you’re ready to make a difference in youth mental health and be part of a collaborative, innovative team, apply now.
For the full position description, visit https://www.orygen.org.au/getmedia/47ef4eef-64d2-4f3c-bcd7-2d9d59c51a33/Sponsor-Operations-Specialist-PD-July-2026-final.pdf.aspx
This is a part or full time (0.8-1.0FTE) 2-year contract.
Applications will close on 31st July (4pm), unless a suitable candidate is found sooner.
Before applying at Orygen, it’s important to understand that you may encounter sensitive information related to mental health as part of your work. Being aware of this and how it could affect you is essential in deciding if this is the right opportunity for you.
Orygen is committed to providing diverse, equitable and inclusive environments for Staff and anyone connected to Orygen. We strive to continue building a culturally safe workplace where our values underpin the way we work and our commitment to First Nations people of Australia, young people and their families, people with disabilities, LGBTIQA+ people and CALD communities. We strongly encourage applications from First Nations people.
Orygen is a child-safe organisation and is committed to promoting and protecting the safety and well-being of all young people and embedding safeguarding practices into all our programs and services. All employment appointments are subject to holding a valid working with children check and successful police check.
Orygen is Australia’s Centre of Excellence in Youth Mental Health and the largest translational research organisation dedicated to youth mental health in the world.
For over 30 years, Orygen has led groundbreaking early intervention and developed evidence-based models of care to improve the mental health outcomes of young people aged 12-25.
About the job
The Clinical Research Associate will contribute to and support the regulatory compliance of Orygen research projects to ensure Good Clinical Practice compliance as well as assist in the development and maintenance of the Quality Management System (QMS). A key aspect of this role is to ensure all research projects across Orygen are conducted in accordance with best practice.
Reporting to the Head of Sponsor Operations you will:
- Study monitoring & reporting - Act as Sponsor CRA/monitor across Orygen-sponsored studies, from the development of risk-based monitoring plans and site visits through to safety oversight and close-out.
- Regulatory & operations advice - Review study documents and guide Investigators and study teams on regulatory compliance, study design, and best practice.
- Systems & quality assurance - Manage serious breaches and CAPA processes, drive SOP development, and support the eTMF roll-out.
- Research governance - Ensure site activities align with Orygen's Research Governance Framework, helping streamline how research is conducted across Orygen-governed sites.
- End-to-end clinical operations - Support studies from start-up and Investigational Product set-up through to eCRF/data management and post-approval reporting.
The following criteria must be met for consideration for this position:
- Minimum bachelor’s degree or comparable qualification in Science, Life Sciences or other Healthcare-related discipline.
- Extensive background in Pharmaceutical, CRO, Biotech, or academic/medical research settings, with hands-on expertise across study start-up, conduct, and close-out (including Teletrials)
- Strong working knowledge of ICH GCP, safety reporting, and implementation of quality systems including QMS processes.
- Skilled in electronic Case Report Forms (e.g. REDCap), Trial Master File management, and review of protocols, PICFs, and study documentation.
- A collaborative, detail-oriented professional who builds effective relationships across internal and external stakeholders, and thrives under pressure with competing priorities.
- $125,000 - $135,000 pro rata + 12% superannuation and $15,900 in NFP salary packaging + $2,600 meals and entertainment card.
- Embrace the freedom of a hybrid work model, combining remote work with on-site collaboration.
- Make a real impact on young people in a dynamic, youth-centered environment.
- Work in a state-of-the-art facility co-designed with young people to advance youth mental health.
- Support Orygen's mission for youth mental health and contribute to positive social change.
If you’re ready to make a difference in youth mental health and be part of a collaborative, innovative team, apply now.
For the full position description, visit https://www.orygen.org.au/getmedia/47ef4eef-64d2-4f3c-bcd7-2d9d59c51a33/Sponsor-Operations-Specialist-PD-July-2026-final.pdf.aspx
This is a part or full time (0.8-1.0FTE) 2-year contract.
Applications will close on 31st July (4pm), unless a suitable candidate is found sooner.
Before applying at Orygen, it’s important to understand that you may encounter sensitive information related to mental health as part of your work. Being aware of this and how it could affect you is essential in deciding if this is the right opportunity for you.
Orygen is committed to providing diverse, equitable and inclusive environments for Staff and anyone connected to Orygen. We strive to continue building a culturally safe workplace where our values underpin the way we work and our commitment to First Nations people of Australia, young people and their families, people with disabilities, LGBTIQA+ people and CALD communities. We strongly encourage applications from First Nations people.
Orygen is a child-safe organisation and is committed to promoting and protecting the safety and well-being of all young people and embedding safeguarding practices into all our programs and services. All employment appointments are subject to holding a valid working with children check and successful police check.
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