Liberte HR is partnering with a US-Headquartered Clinical Research Organisation to appoint a CRA II to support their growing Australia-based clinical operations team.

This is an exciting opportunity to join a growing Clinical Operations Team in Australia with strong financial backing and a strong established presence in US, Europe and APAC.

The Role:

- Manage assigned clinical trial sites from site selection through close-out
- Conduct pre-study, site initiation, routine monitoring, and close-out visits
- Ensure protocol compliance, data integrity, safety reporting, and GCP standards
- Support site start-up activities including EC submissions and essential documentation
- Track recruitment, resolve site issues, and ensure timely study execution
- Collaborate closely with project teams and provide ongoing site training and support
- Maintain accurate documentation within TMF/CTMS and study systems

Requirements:





- Degree in Life Sciences, Pharmacy, Nursing, or related discipline
- Proven experience as a Clinical Research Associate with at least 2 years experience for independent site monitoring in Australia.
- Experience with monitoring trials in Oncology, Cardio-Metabolic, and/Haematology will be beneficial.
- Solid knowledge of ICH-GCP, monitoring practices, and site management
- Experience with site start-up and independent site monitoring
- Highly organised with the ability to manage multiple sites and priorities
- Confident communicator with strong stakeholder and site relationship skills
- Willingness to travel intrastate and interstate in Australia; valid driver’s licence required
- Full Working Rights in Australia

📌 Clinical Research Associate II (Sydney)
🏢 Liberte HR Services
📍 Sydney