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 on-site CRA roles within Sponsor or CRO environments, with solid 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 (Victoria)
🏢 Sironax
📍 Victoria
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