An exciting opportunity for a Clinical Project Associate to work within an innovative MedTech environment combining clinical research, medical imaging and AI-driven technology.
You’ll support the planning and delivery of clinical studies and research projects that contribute to AI development, regulatory submissions and scientific publications.
This is a great opportunity for someone who enjoys the operational side of clinical research but also wants exposure to technology, product development and medical imaging.
What You’ll Be Doing
- Support the day-to-day delivery of clinical studies and research projects.
- Coordinate with CROs, clinical sites, investigators and external vendors.
- Assist with study start-up, monitoring, project tracking and reporting.
- Support the development of study protocols, project plans, training materials and regulatory documentation.
- Assist with image and clinical data management processes.
- Monitor study deviations, trends, data readiness and data quality.
- Maintain accurate study documentation and applicable Trial Master Files (TMF).
- Collaborate across Clinical Development, R&D and Quality/Regulatory teams.
- Depending on your background and training, contribute to cardiac CT image analysis and image-analysis methodology development.
Ideally, you’ll have:
- A Bachelor's degree in Life Sciences, Biomedical Engineering or a related discipline.
- 3+ years of relevant professional experience.
- Around 1–3 years' experience in project management involving clinical research or other research projects.
- Familiarity with international clinical research regulations and ethical standards, including ICH-GCP.
- Strong organisational skills and attention to detail.
- MS Word and Excel proficiency; MS Project exposure would be beneficial.
You could be working as a:
Clinical Research Associate | Clinical Trial Associate | Clinical Project Coordinator | Clinical Research Coordinator | Biomedical Engineer | Research Project Officer
You don't necessarily need to come from a traditional pharmaceutical clinical-trials pathway. Prior clinical research experience is preferred.
Why Consider It?
You're not simply coordinating traditional clinical trials — you're helping deliver research that supports AI development, regulatory evidence and scientific publications, while working alongside R&D and regulatory teams.
Some flexibility around working hours is required to collaborate between Western Australia and the US, and occasional travel may be required.
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Project Associate employer: Lead Group
This business advisory firm in Melbourne is an exceptional employer, offering a supportive work culture that prioritises employee growth and development. With structured training events, flexible work hours, and a strong emphasis on work-life balance, employees are encouraged to enhance their skills while enjoying a vibrant social club and fitness activities. Joining this team means being part of a collaborative environment where your contributions are valued and career progression is actively supported.
