pPSI 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.
/ppThe candidate should have a scientific degree, English and Italian proficiency, strong MS Office skills, and a detail-oriented, collaborative mindset to support regulatory workflows /p #J-*****-Ljbffr
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