Senior Biostatistician

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Job description

Job Overview:Senior Biostatistician required to work for Labcorp Drug Development in a Lead roleWorking with multiple Sponsors across several therapeutic areas in all phases of clinical trialsThis is a permanent full-time role, either office based or home based anywhere in Europe or in South AfricaYou must have some previous experience of Leading studies as a Biostatistician in either a biotech, CRO or pharma companyJoin 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 therapeutic areas, leading projects and mentoring junior members of the department. 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.Job Primary FunctionsPerform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetingsPerform project management activities for identified projects including resource planning, timelines and milestone managementPreparation of Statistical Analysis Plans (including mock TFL shells) for medium complexity studies under the supervision of more senior statistical staffPerform complex statistical analyses, quality check statistical analyses developed by other statisticiansConduct overall statistical review of TFLs for complex studies prior to client deliveryReview CRF and other study specific specifications and plansMay perform sample size calculation for simple studies under the supervision of more senior statistical staffDevelop the statistical sections of the protocol for simple to medium complexity studies under the supervision of a statistical consultantProvide statistical input and review of the CSR for medium complexity studiesPreparation and review of randomization specifications and generation of randomization schedulesMentor of biostatisticians within project activities; assigned tasks related to the development of staff within the departmentPresent and share knowledge at team meetings and/or at monthly seminarsAttend bid defense meetings for medium complexity studies in order to win new businessRepresent the department during project-driven client audits.Education/Qualifications:Master's degree, equivalent, or higher in Biostatistics or related fieldExperience:You must have some previous experience of Leading studies as a Biostatistician in either a biotech, CRO or pharma companyAbility 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 analysisAbility to effectively communicate statistical conceptsA good knowledge of the overall clinical trial processExperience in the preparation of Statistical Analysis Plans, analysis, reporting, etcYou must be fluent in English language (both verbal and written)NO AGENCIES PLEASEMORE INFORMATION AVAILABLE ON REQUESTFor a confidential discussion about this opportunity, please phone Peter Lewis on To apply, please click on the APPLY button.Keywords:Labcorp Drug Development, Covance By Labcorp, Covance, Chiltern, FSP, Functional Service Provision, Clinical Analytics, FSPx, 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, CDISC, SDTM ADaM, "Statistical Analysis Plan", 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