Jobtailor is seeking a Regulatory Affairs professional in Espoo to support regulatory submissions, coordinate eCTD publishing, and ensure documents are compliant throughout lifecycle. You will collaborate with Clinical Development, Operations, Medical Writing, and CRO partners; assist preparation for health authority interactions (EMA/FDA) and maintain trackers.

The ideal candidate has 2+ years in regulatory affairs in pharma/biotech, knowledge of CTA/CTIS, and strong English, with attention to