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, 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.
* Strong 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