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Assessor - Clinical Assessment, Human Products Authorisation and Registration / Measúnóir - Measúnú Cliniciúil, Táirgí don Duine a Údarú agus a Chlárú

Salary €77,045 - €89,345 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.

Reporting to a senior member of the Human Product Authorisation and Registration (HPAR) Department, the Clinical Assessor will be responsible for the assessment of the clinical components of licensing applications. This will include analysis of the efficacy and safety data from clinical trials and to a lesser extent pharmacokinetic and biopharmaceutical studies supporting these applications. The assessment requires an ability to interpret complex clinical datasets and make an informed decision on the overall benefit risk analysis of a medicine. The assessor will also be tasked with writing detailed clinical assessment reports as part of the EU medicines regulatory review process.

The assessment of clinical medicinal products submitted through the centralised authorisation procedure (through the European Medicines Agency) will be the main area of responsibility but other opportunities to assess other types of authorisation applications or clinical trial applications may arise from time to time.

 

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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