25 sep
|
Ergomed
|
Madrid
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.
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