Biostatistician

BiostatisticianOur client, a national regulatory body are currently recruiting for a Biostatistician to join their team. In this role, you will use your statistical and professional expertise to lead the assessment and review of the statistical aspects of marketing authorisation applications and clinical trial applications. You will critically analyse complex clinical and scientific information, making sound judgements on the value of the statistical methodologies employed, and write informative assessment reports for a multi-disciplinary readership. You will provide expertise on good drug development, interacting with medical colleagues, multi-disciplinary advisory committees and company representatives and will provide in-house statistical expertise to other technical sections in the organisation. This role offers hybrid working-2 days per week in the Dublin office and three days working from home.Responsibilities Analyse and critically appraise statistical aspects of pre-marketing applications including dossiers for medicines, scientific advice applications and clinical trial applications and prepare assessment reports. Assessment includes, but is not limited to, statistical methods, statistical design, statistical analyses plans, sample size and sensitivity analyses and imputation methods for missing dataLiaise with assessment teams in the assessment of the above-mentioned applicationsInform and influence National and EU advisory and decision-making committeesProvide advice to the organisation and to National or EU scientific committeesContribute to the peer review of national and EU scientific evaluation documentsProvide statistical advice on behalf of the organisation to stakeholders such as investigators, sponsors, and others to ensure that any planned study/project results and conclusions are presented accurately and without biasRepresent the organisation at relevant National and EU meetings, when requiredMaintain and enhance personal and technical competence by keeping abreast of new statistical methodologyContribute to and assist in the delivery of statistical training and knowledge sharingProvide data analysis to support policy direction, and other functions as may be determined depending on the needs of the Strategic Objectives of the organisationSupport the Section Manager, and Section Leadership Team in the on-going development of the sectionProvide support and input to colleagues and others within the Section and the departmentParticipate in shaping the organisation, strategic visioning, developing the business, innovating and creating Operational Objectives Requirements A postgraduate qualification (MSc/PhD) (NFQ level 9 or 10) in statistics, medical statistics or biostatisticsA relevant 3rd level honours degree (NFQ level 8) in mathematical, life science, or healthcare discipline (e.g. mathematics/applied mathematics, biostatistics, statistics, biomedical science, pharmacology, pharmacy, genomics, psychology)Experience employing analytical thinking on complex data and statistics, and ability to make appropriate and tailored recommendations, comprehensible by multidisciplinary audienceHave a sound understanding of statistical methodology relevant to the regulation of medicines and clinical trials, and emerging methodologies relevant to the field of statistics and medicines regulationKnowledge and understanding of the drug development process (pre-clinical, quality, clinical and post-approval) with understanding of drug development as a continuumKnowledge and understanding of the clinical trial process, different clinical trial designs and various statistical approaches that may be usedExperience and knowledge with statistical software packages, standard office software (Word, Excel, PowerPoint), cloud-based platforms (Microsoft Teams) and communication tools (Outlook)Ability to evaluate and critically appraise complex information from a variety of sources and make effective decisionsSelf-starter, accountable, capable of effective communication, negotiation and decision makingStrong organisational skills, including the ability to prioritise workloadExcellent oral and written communication skills, excellent attention to detailPassion for knowledge sharing and dissemination of statistical expertise, and a willingness to contribute to peer-to-peer learning.The ability to work as part of a cross-functional team and clearly communicate statistical issues and methods to multidisciplinary audiences In addition, the following would be considered an advantage: Experience in applying statistical methods in biomedical research, pharmaceutical or CRO industry or drug regulatory agencyMotivated to quickly develop a sound understanding of a wide range of statistical and clinical trial methodology, including state-of-the-art techniques, relevant to the regulation of medicinal products across the breadth of the drug development processKnowledge and experience of centralised licensing and clinical trials regulatory processes *A more comprehensive role profile can be provided upon request*