PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations. The candidate should have a scientific degree, English and Italian proficiency, strong MS Office skills, and a detail-oriented, collaborative mindset to support regulatory workflows J-18808-Ljbffr
📌 Regulatory Specialist: CTR Italy, Hybrid (Milano)
🏢 Altro
📍 Milano