TFS HealthScience is seeking an EU Director, Regulatory Affairs to lead regulatory strategy across device and drug development, working within the CDS Unit. This senior role focuses on EU CTR/CTIS programs and general regulatory initiatives, coordinating with study start-up and business units to optimize submissions and timelines. Based in Europe, you will influence regulatory approaches for clinical investigations, orphan designation, pediatric plans, and scientific advice meetings, while
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📌 EU Director, Regulatory Affairs – Drug & Device Strategy (Málaga)
🏢 TFS HealthScience
📍 Málaga
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