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.
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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 New South Wales (Australia)
🏢 ARTO
📍 Australia
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