Flexible Working
Learning & Development
Wellbeing

Assessor, Methodology (Pharmacokinetics) - Centralised and Clinical Trials Licensing - HPAR

Salary €74,779 - €86,717 per annum
Location Hybrid
{Mergefield Value}
{Mergefield Value}

This is a Temporary, Full Time vacancy that will close in {x} days at {xx:xx} BST.

The Human Products Authorisation and Registration Department provides human medicines licensing services to the HPRA. The department is structured with two main technical sections - one delivering assessments for products authorised through the centralised (EU) mechanism and for clinical trials and the other delivering assessments for products authorised through mutual recognition, decentralised and national mechanisms.

The Methodology team is part of the Centralised & Clinical Trials Licensing section that delivers assessments for products authorised through the centralised (EU) mechanism and for clinical trials. This team comprises a methodology team consisting of clinical pharmacology and statistical assessors. The Assessor, Methodology (pharmacokinetics) will report to the Executive Assessor (Methodology) team lead.

The Assessor, Methodology (pharmacokinetics) will use their scientific and professional expertise to lead assessments of the clinical pharmacology aspects of marketing authorisation applications and clinical trial applications. The assessment involves extensive report writing, contributing to the benefit risk assessment and making recommendations.

The Assessor, Methodology (pharmacokinetics) will be expected to critically analyse both clinical & complex scientific information, make sound judgments on its value and write informative reports for a multi-disciplinary readership.

The Assessor, Methodology (pharmacokinetics) will work closely and maintain effective working relationships with other members of the section, and with members of the HPAR department as a whole, 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.

The Assessor, Methodology (pharmacokinetics) will maintain effective working relationships with colleagues in other sections and departments of the HPRA, to ensure that issues requiring cross-functional input are conducted effectively and followed up on.

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.

Alternatively, please sign in with...


Published

Not Published

Closing

in X days

{Expiry}