Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products, while taking a step further in your professional career.
Hybrid working arrangement in Milan area
Your role:
Support country-level regulatory activities for Italy under the EU Clinical Trials Regulation (CTR)Prepare and coordinate CTR Part II submission
📌 Regulatory Officer. (Milano)
🏢 Psi
📍 Milano
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