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Senior Medical Officer (Acting) - Centralised and Clinical Trials Licensing, HPAR / Oifigeach Eolaíochta (Gníomhach) - Ceadúnú Trialacha Láraithe agus Cliniciúla, HPAR

Salary €117,275 - €130,829
Location Hybrid
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This is a Temporary, Full Time vacancy that will close in {x} days at {xx:xx} BST.

The Human Products Authorisation and Registration (HPAR) Department is responsible for delivering human medicines licensing services on behalf of the HPRA. The department comprises two principal technical sections. The Centralised and Clinical Trial Licensing Section undertakes assessments for products authorised via the EU centralised procedure and EU clinical trial assessments, while the National Licensing Section conducts assessments for products authorised through mutual recognition, decentralised, and national procedures.

In terms of centralised assessments, our strategy is to focus on the following therapeutic areas: respiratory, dermatology, ophthalmology, rheumatology, immunology and for clinical trials, there is a requirement for oncology expertise. We also have an Advanced Therapy Medicinal Products (ATMP) and rare diseases portfolio.

The Senior Medical Officer (SMO) will be a therapeutic area lead for their area of specialisation, ensuring the strategy, operations and capability of the department is aligned to current clinical and regulatory developments in that therapeutic area on a continuous basis.

The SMO role operates at the organisational level, ensuring the successful execution of strategies and contributing to long-term organisational sustainability and success. The SMO will develop and shape organisational frameworks that align with strategic priorities and improve overall efficiency. The SMO will be expected to display competencies at a strategic level relating to leadership, knowledge sharing, learning & growth, strategic thinking & impact and organisational awareness

The SMO will work closely with and maintain effective working relationships with other members of the Centralised and Clinical Trial Licensing section, and colleagues across the organisation, to ensure effective co-ordination and co-operation across all areas of assessment and to ensure that the objectives of the HPAR department are met.

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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