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Scientific Officer, Vigilance Assessment - Human Products Monitoring/Oifigeach Eolaíochta, Measúnú Forairdill - Monatóireacht ar Earraí le nÚsáid ag an Duine

Salary €44,831-€74,404
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 post is located within the Human Products Monitoring (HPM) department contributing to the evaluation of pharmacovigilance data, safety monitoring and risk management relating to medicines. 

The Scientific Officer will contribute to the technical functions of Vigilance Assessment (VGA) section and support risk-based assessment activities through data management and analysis activities.

The Scientific Officer will perform signal detection activities including preliminary analysis and evaluation of data arising from available databases and scientific literature with integration of qualitative and quantitative approaches in accordance with EU guidance to support further assessment and management of signals. This will also involve ensuring that the outcomes of EU signal recommendations are communicated to market authorisation holders where appropriate and implemented nationally in accordance with standard procedures.

The Scientific Officer will perform assessment of Risk Management Plans (RMPs) submitted in relation to medicinal products authorised through national procedures and will support the VGA assessment team in assessment procedures undertaken by the HPRA at EU level, including RMP and EU PSUR single assessments.

The Scientific officer will support the tracking of key activities, actions and outcomes for the VGA section relating to signal management and recommendations, medicines safety issues and horizon scanning activities as required.

The Scientific Officer will also co-ordinate and support the provision of technical training within the VGA section including development and updating of section training plans, training plan templates, internal training tools and resources for the VGA section in key areas and providing support for continuous professional development activities within the section.

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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