Ergomed, a specialist clinical research organisation, is seeking a Specialist, Study Start Up and Regulatory Affairs to lead and coordinate study start up and regulatory activities across multiple countries, ensuring regulatory compliance and timely site initiation. xcskxlj
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You will draft and review essential documents, manage country-specific regulatory submissions, translations, and agreements, and provide strategic input to clients and internal teams to protect timelines and data quality.
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📌 Global Study Start-Up & Regulatory Lead (Madrid)
🏢 Ergomed
📍 Madrid
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