ARTO is seeking a Senior Clinical Research Associate to lead site selection and regulatory submissions for an international randomized clinical trial spanning Europe and the United States. The role will operate without a full CRO model, with key activities managed internally.
You will oversee site onboarding, informed consent preparation, and regulatory package development. You will adapt documents to local requirements and coordinate translations, providing country-specific regulatory guidance
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📌 Senior Cra – Global Rcts & Regulatory Submissions (Sydney)
🏢 ARTO
📍 Sydney
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