Senior Statistical Programmer (CDS)

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Job description

Job Overview:Senior Statistical Programmer required to work for Labcorp Drug Development as a Lead Statistical ProgrammerYou will be employed by Labcorp Drug Development working in our Clinical Development Services (PII-IV) group with the opportunity to work across multiple Sponsors and therapeutic areasHome based anywhere in Europe or South AfricaYou must have previous experience of working as a Statistical Programmer in either a biotech, CRO or pharma companyCandidates must be fluent in English language (both verbal and written)Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Senior Statistical Programmer. You will work in our Clinical Development Services group so you will enjoy a varied role working for different sponsors across several therapeutic areas within phases II-IV. The position offers a strong support network, 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. This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.Job Primary FunctionsPerform the role of the Lead Statistical ProgrammerPlan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc.Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLsProduce Define XML/PDFs, Analysis Results Metadata (ARM), annotated CRFs and Reviewers Guides to support SDTMs and ADaMsDevelop specifications for SDTMs and ADaM datasetsReview SAPs and TFL shells from a programming perspective for studiesMentor less-experienced programmers in the processes around SDTMs, ADaMs and TFLsPresent and share knowledge at department meetingsRespond to QA and client audits, and support qualification auditsIdentify processes within programming that will increase productivity, quality and efficiencyEducation/Qualifications:BSc, preferably in computing, life science, mathematical or statistical subjectExperience:You must have some previous experience of working as a Lead Statistical Programmer in either a biotech, CRO or pharma company using SAS.Knowledge of CDISC requirementsPositive attitude and willingness to learn and contribute in a team setting and communicate effectively within the team environmentGood organization skills and the ability to prioritize own workSelf motivation and ability to work independentlyA cooperative and team-oriented approachCandidates 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 (0) . To apply, please click on the APPLY button.Keywords:Labcorp Drug Development, Covance by Labcorp, Lead Statistical Programmer, Senior Statistical Programmer, Covance, Statistical programming, Chiltern, Covance, Phases I-IV, Programmer Analyst, Stats Programmer, Senior, Statistical Programmer, Lead SAS Programmer, CDISC, ADaM, SDTM, Biostatistics, Senior Statistician, Biostatistician, Statistics, Study Biostatistician, pharma, pharmaceutical, SAS, STAT, home based, pharma, pharmaceutical, home-based, flexible working, flexible location, home based, field based, home based EU Anywhere, anywhere in Europe, field-based, United Kingdom, UK, Great Britain, England, Maidenhead, Reading, Berkshire, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Northern Ireland, Austria, Belgium, Bulgaria, Czech Republic, France, Paris, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Leiden, Poland, Portugal, Romania, Russia, Slovakia, Bloemfontein, Centurion, South Africa, Madrid, Barcelona, Spain, Ukraine, oncology, cancer, #LI-PL1, #LI-Remote, Remote, EMEA