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Senior Biostatistician (CDS)

Laboratory Corporation of America Holdings (Covance)

Brussels, Belgium

<h2>Job Overview:</h2><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: black;">Senior Biostatistician r</span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">equired to work for Labcorp Drug Development in a Lead role</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Working with multiple Sponsors across several therapeutic areas in all phases of clinical trials</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">This is a permanent full-time role, either office based or home based anywhere in </span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Europe or in South Africa</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">You must have some previous experience of Leading studies as a Biostatistician in either a biotech, CRO or pharma company</span></li></ul><p style="margin: 0px;"><span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Senior Biostatistician.  You will enjoy a varied role working for different sponsors across several </span></span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">therapeutic<span><span style="font-family: 'Arial',sans-serif;"> areas, leading projects and mentoring junior members of the department.  </span></span>The position offers an excellent support network with access to Labcorp Drug Development’s statistical consultants, flexible working solutions and the opportunity to progress your career.  If you are looking to strengthen your Lead expertise within a varied and dynamic environment, then this is a fantastic opportunity.  </span></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Job Primary Functions</span></u></strong></p><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Perform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Perform project management activities for identified projects including resource planning, timelines and milestone management</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Preparation of Statistical Analysis Plans (including mock TFL shells) for medium complexity studies under the supervision of more senior statistical staff</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Perform complex statistical analyses, quality check statistical analyses developed by other statisticians</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Conduct overall statistical review of TFLs for complex studies prior to client delivery</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Review CRF and other study specific specifications and plans</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">May perform sample size calculation for simple studies under the supervision of more senior statistical staff</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Develop the statistical sections of the protocol for simple to medium complexity studies under the supervision of a statistical consultant</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Provide statistical input and review of the CSR for medium complexity studies</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Preparation and review of randomization specifications and generation of randomization schedules</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Mentor of biostatisticians within project activities; assigned tasks related to the development of staff within the department</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Present and share knowledge at team meetings and/or at monthly seminars</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Attend bid defense meetings for medium complexity studies in order to win new business</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Represent the department during project-driven client audits.</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Master’s degree, equivalent, or higher in Biostatistics or related field</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">You must have some previous experience of Leading studies as a Biostatistician in either a biotech, CRO or pharma company</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Ability to program in one or more statistical software packages (SAS®) used to conduct statistical analyses. SAS proficiency including use of a variety of statistical procedures e.g., non-parametric analysis, linear and non-linear models, categorical data and survival analysis</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Ability to effectively communicate statistical concepts</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">A good knowledge of the overall clinical trial process </span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Experience in the preparation of Statistical Analysis Plans, analysis, reporting, etc</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">You must be fluent in English language (both verbal and written)</span></li></ul><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">NO AGENCIES PLEASE</span></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0cm; margin-bottom: .0001pt;"><strong><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: black;">MORE INFORMATION AVAILABLE ON REQUEST</span></strong></p><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: black;">For a confidential discussion about this opportunity, please phone Peter Lewis on </span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: black;">+44 7917 710 602 </span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: black;">To apply, please click on the APPLY button.  </span></p><p style="margin: 0cm; margin-bottom: .0001pt;"> </p><p style="margin: 0px;"><strong><u><span style="font-size: 8.0pt; font-family: 'Arial',sans-serif;">Keywords:</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 8.0pt; font-family: 'Arial',sans-serif;">Labcorp Drug Development, Covance By Labcorp, Covance, Chiltern, FSP, Functional Service Provision, Clinical Analytics, FSPx, </span><span style="font-size: 8.0pt; font-family: 'Arial',sans-serif;">Statistician, Biostatistician, Stato, Statistics, Senior Biostatistician, Lead Biostatistician, Study Biostatistician, pharma, pharmaceutical, Bloemfontein, Vienna, Brussels, Sofia, Prague, Paris, Berlin, Athens, Budapest, Dublin, Rome, Vilnius, Amsterdam, Warsaw, Lisbon, Bucharest, Moscow, Bratislava, Madrid, Bern, Basel, Kiev, Slough, Berkshire, London, England, Edinburgh, United Kingdom, Cambridge, Swansea, Sheffield, Manchester, Alderley Edge, Birmingham, home based, field based, home-based UK Anywhere, anywhere in England, anywhere in Scotland, anywhere in Wales, anywhere in Ireland, flexible location, <span style="color: black;">CDISC, SDTM ADaM, “Statistical Analysis Plan”, </span>study protocols, clinical study reports, integrated summary of safety and efficacy reports, Investigator Brochures, periodic safety update reports, oncology, rare diseases, Europe, cancer, Austria, Belgium, Bulgaria, Czech Republic, France, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Poland, Portugal, Romania, Russia, Slovakia, Spain, Switzerland, Ukraine, South Africa, #LI-PL1, #LI-Remote, Remote, EMEA</span></p>

Job posted: 2021-12-17

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