Allucent is seeking an experienced Regulatory Affairs Coordinator to support site start-up activities for clinical trials. You will manage regulatory documents, track milestones in CTMS/eTMF, and prepare local submissions to regulators in coordination with the Global Regulatory team.
A Life Science degree and 2+ years in regulatory affairs are required, with fluency in Italian and English. The role offers flexible hours, competitive salaries per location, and growth opportunities within Allucent.
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