Worldwide Clinical Trials is a integral CRO seeking a senior Regulatory Affairs professional to lead regulatory submissions across EMEA, Asia Pacific, and Latin America, ensuring ongoing compliance with evolving regulations and key regulatory documents.
You will coordinate ethics submissions, provide strategic regulatory guidance, and mentor junior staff while partnering with sponsors and project teams to drive timely regulatory outcomes.
📌 Global Regulatory Affairs Manager – Submissions (Madrid)
🏢 Worldwide Clinical Trials
📍 Madrid
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