Sironax is seeking a proactive Clinical Research Associate to oversee on-site monitoring of clinical trial sites in Australia. The role ensures protocol adherence, IP accountability, and TMF readiness, interfacing with investigators and site staff.
Experience includes 2–4 years in in office CRA roles within Sponsor or CRO environments, with strong knowledge of ICH-GCP and Australian regulations (TGA). University degree in Life Sciences or related field is required.
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📌 Australia CRA: On‑Site Monitoring & Trial Excellence
🏢 Sironax
📍 Australia
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