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Scientific Officer (Acting), Centralised Clinical Trial Licensing Section, HPAR / Oifigeach Eolaíochta (Gníomhach), Ceadúnú Trialacha Láraithe agus Cliniciúla, HPAR

Salary €45,279 - €75,148 per annum
Location Hybrid
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This is a Temporary, Full Time vacancy that will close in {x} days at {xx:xx} BST.

The Scientific Officer supports the regulation, scientific evaluation, and authorisation (i.e., licensing) of human medicinal products within Ireland and the European Union. The role combines regulatory project management, scientific assessment, operational coordination, and process improvement activities to facilitate the effective and efficient authorisation of medicines through centralised European regulatory procedures. The post also provides operational support to Irish representatives involved in the European Medicines Agency’s scientific committees.

Essential Criteria:

  • A third level degree in a relevant scientific discipline (e.g., pharmacy, biomedical science)
  • A minimum of one years’ relevant experience in an academic, healthcare, industry or regulatory environment relating to medicinal products
  • Strong interest in developing knowledge and understanding of the operation of the European Medicines Regulatory Network
  • Relevant experience in the collation, evaluation and presentation of scientific data
  • Proficient with use of Microsoft Word, Excel, PowerPoint, and Outlook

Closing date for applications: 18th October 2026

Interviews are expected to be held week commencing 2nd November 2026.

We are the Health Products Regulatory Authority (HPRA) and we regulate medicines and devices for the benefit of people and animals. We are committed to excellence in health product regulation through science, collaboration and innovation.

Our remit and regulatory functions include human and veterinary medicines, clinical trials, medical devices, controlled drugs, blood and blood components, tissues and cells, and cosmetic products.

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