Data Processor/Cough Analyst, Clinical Trials- Vitalograph, Limerick

  • Limerick
  • Vitalograph
<p class="ql-align-justify"><strong>Data Processor/Cough Analyst, Clinical Trials- Vitalograph Ireland, Limerick. </strong></p><p class="ql-align-justify"><strong>&nbsp;</strong></p><ul><li class="ql-align-justify"><strong>Full-time role</strong></li><li class="ql-align-justify"><strong>Progression opportunities available</strong></li><li class="ql-align-justify"><strong>Full training provided</strong></li></ul><p class="ql-align-justify"><strong>&nbsp;</strong></p><p class="ql-align-justify"><strong>About Vitalograph</strong></p><p class="ql-align-justify">&nbsp;</p><p class="ql-align-justify">Vitalograph is a leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders, and advanced high-reliability equipment and software systems used in respiratory end-point clinical drug trials.&nbsp;We have designed, developed and manufactured respiratory diagnostic devices, software, and consumables for healthcare professionals, for 60 years. Headquartered in the UK, Vitalograph has operations in Ireland, Germany, and the USA.&nbsp;</p><p class="ql-align-justify"><strong>&nbsp;</strong></p><p class="ql-align-justify">Vitalograph's custom solutions and a personalised approach to Clinical Trials means we can meet a wide range of respiratory clinical study needs, with services including project and data management, data analysis, clinical over-reading, training, software configuration, eCOA and site support.</p><p class="ql-align-justify">&nbsp;</p><p class="ql-align-justify">Reporting to the Cough Analysis Supervisor/Team Leader, the Cough Analyst will work with the Cough Analysis Team reviewing audio data from files generated from one of the company's medical devices.&nbsp;</p><p class="ql-align-justify">&nbsp;</p><p class="ql-align-justify"><strong>Role requirements:</strong></p><p class="ql-align-justify"><strong>&nbsp;</strong></p><p class="ql-align-justify"><strong>Duties include but are not limited to.</strong></p><p class="ql-align-justify"><strong>&nbsp;</strong></p><ul><li class="ql-align-justify">Analyse/process data gathered by one of the company's medical devices during the clinical trial process.</li><li class="ql-align-justify">Review of work to ensure a high level of quality is maintained.</li><li class="ql-align-justify">Communicate effectively with internal team to ensure team &amp; project deadlines are met.</li><li class="ql-align-justify"><br></li></ul><p class="ql-align-justify"><strong><u>Minimum Requirements:</u></strong></p><p class="ql-align-justify"><strong>&nbsp;</strong></p><ul><li class="ql-align-justify">Attention to detail with capability for high levels of focus and concentration for long periods.</li><li class="ql-align-justify">Hard working, motivated, reliable with a good attitude towards their co-workers.</li><li class="ql-align-justify">Excellent timekeeping and attendance.</li><li class="ql-align-justify">Competent person, capable of working under their own initiative with minimal supervision and a good team player.</li><li class="ql-align-justify">Computer literate with experience using MS Word &amp; Excel.</li><li class="ql-align-justify"><strong>Full training will be provided in this role.</strong></li></ul><p class="ql-align-justify">&nbsp;</p><p class="ql-align-justify"><strong><u>Key competencies:</u></strong></p><p class="ql-align-justify">&nbsp;</p><ul><li class="ql-align-justify">Excellent written and verbal communication and interpersonal skills.</li><li class="ql-align-justify">Ability to work with others in a spirit of good will and cooperation.</li></ul><p><br></p>