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 robust 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.
Robust 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 robust stakeholder and site relationship skills
Willingness to travel intrastate and interstate in Australia; valid driver's licence required

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