TRIUM Clinical Consulting NV is seeking an experienced Consultant Regulatory Affairs & Publishing to lead European regulatory submissions, strategy, and lifecycle management of medicinal products. Hybrid Madrid or Warsaw, full-time role.
You will coordinate Module 1, eCTD dossiers, interact with Health Authorities, and guide cross-functional teams. Requires 6–8 years in regulatory affairs, EU knowledge, and proven submission experience.
📌 Strategic Regulatory Affairs (Pozuelo de Alarcón)
🏢 TRIUM Clinical Consulting
📍 Pozuelo de Alarcón
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