Job Description
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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