Full TimeENAsia/Pacific
Epworth is an innovator in Australia’s health system, embracing the latest in evidence-based medicine to pioneer treatments and services for our patients. At Epworth, we are united in our commitment to fostering a diverse and inclusive workplace—one that is culturally safe and respectful of the enduring cultural and spiritual connections of our people.
We value all differences, ensure equitable practices, and empower individuals to lead and learn inclusively in their everyday interactions. Our goal is to create an environment where everyone feels a genuine sense of belonging.
Our values and purpose define Epworth's approach and delivery. We pride ourselves on communicating and delivering them in a real and meaningful way. Every Patient Matters.
Clinical Research Coordinator – Julia Argyrou Endometriosis Centre
Full-time | Fixed-term (12 months)
Epworth HealthCare is Victoria’s largest not-for-profit private health care group, renowned for excellence in patient care, research and innovation. We are seeking an experienced Clinical Research Coordinator to support high‑quality investigator‑initiated and sponsored research at the Julia Argyrou Endometriosis Centre at Epworth, based in Richmond.
The Opportunity
This role provides end-to-end coordination of clinical research projects focused on improving health outcomes for people affected by endometriosis. Working closely with Centre Directors, clinicians, researchers and external partners, you will support the design, delivery and governance of clinical research activity across the Centre.
Reporting to the Centre Program Manager, Argyrou Endometriosis Centre, you will play a key role in ensuring studies are delivered efficiently, ethically and in compliance with regulatory and governance requirements, while contributing to the Centre’s research excellence and growth.
Key Responsibilities
Position Description Inherent Requirements
About You
You are an organised, detail-oriented and collaborative research professional with experience coordinating clinical research in a healthcare or research environment. You are comfortable working across multiple studies and stakeholders while maintaining high standards of quality and compliance.
You will bring:
At Epworth, it’s a community
At Epworth, Every Patient Matters. You’ll join a values-driven organisation committed to advancing patient care through innovation, research and collaboration. This role offers the opportunity to contribute to meaningful research, work with leading clinicians, and be part of a supportive, high-performing research environment.
In addition to this, you will have access to:
We welcome applicants from all backgrounds. This includes First Nations peoples, people with disability, mature-age and young job seekers, members of the LGBTIQA+ community, and individuals from all cultural backgrounds. We are committed to providing an equitable, inclusive, and barrier-free recruitment experience for everyone.
If you need support during the application process or would like to discuss reasonable adjustments, we encourage you to let us know what you need to participate fully and confidently. We understand that sharing your needs can feel daunting, so please know that any information you provide will be treated with the utmost confidentiality and respect.
Ready to Make a Difference?
Apply now! Click I’m Interested and submit your CV and cover letter as a single document including brief responses to the the following selection criteria questions.
Application Requirements
As part of the application process, please also respond to the following selection criteria questions in your cover letter:
Clinical Research Experience
Do you have a minimum of two (2) years’ experience working as a Clinical Research Coordinator or in an equivalent clinical research role?
Ethics & Governance Experience
Please describe your experience preparing and managing Human Research Ethics Committee (HREC) and research governance submissions, including National Mutual Acceptance (NMA) where applicable.
Regulatory & GCP Knowledge
Do you have current Good Clinical Practice (GCP) training and experience working in accordance with ICH GCP and the National Statement on Ethical Conduct in Human Research?
Study Coordination & Workload Management
Briefly outline your experience coordinating multiple clinical research studies simultaneously, including how you manage competing priorities and deadlines.
Database & Data Management Experience
Please describe your experience with research databases, such as managing or maintaining REDCap databases.
Availability to Commence / Notice Period
Please advise your availability to commence employment and any notice period required.
Salary Expectations
Please outline your salary expectations (exclusive of superannuation).
Interview Availability
Please indicate your availability to attend an interview over the coming weeks.
Early applications are encouraged — shortlisting will commence immediately.
For further information about the role, please refer to the attached Position Description or contact talent@epworth.org.au.
Apply now… we’ve over 8,000 perspectives at Epworth and we’re ready to welcome yours!
It is a condition of employment with Epworth HealthCare, subject to reasonable exemptions, that you have had an annual Influenza vaccination, where this is required under Epworth policy.
As a child safe organisation, all successful applicants are required to satisfactorily clear a National Police Check (conducted by Epworth) and may be required to hold a valid employee Working with Children Check (provided by you).
At Epworth, we believe inclusion and diversity are essential to our culture and values. We focus on fairness and opportunity for all – across race, ability, ethnicity, gender, age, sexuality, cultures and beliefs – that reflect the communities we work in. At Epworth, we care.
