Upsilon Global is seeking an accomplished Clinical Regulatory Director with 10–12 years of regulatory affairs experience to lead global regulatory strategies and high‑performing teams across multiple development programs.
You will drive European CP, MRP and DCP submissions, oversee post‑approval lifecycle management, and partner with clinical, medical, quality and commercial teams to accelerate innovative therapies to patients worldwide.
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📌 Global Regulatory Affairs Leader: Eu Strategy & Submissions (Milano)
🏢 Upsilon Global
📍 Milano
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