Principal Statistical Programmer Sas Or R Mid Sized Cro Oncology And Rare Diseases Focused Remote Job In Sheffield

Principal Statistical Programmer (SAS OR R), Mid-Sized CRO, Oncology and Rare Diseases Focused - Remote - Meet
  • Sheffield, Other, United Kingdom
  • via Test Feed 1
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Job Description

Principal Statistical Programmer (SAS OR R), Mid-Sized CRO, Oncology and Rare Diseases Focused - RemoteA chance to join one of the world’s most successful life-science companies has become available for a Principal/Senior II Statistical Programmer.Here you will be a part of the Global Programming Division, where you will be responsible for leading multiple complex projects in oncology and other therapeutic areas – clinical phases I-III.This company offers real chances of progression to the management level, with a tailored development program in place for Principal Programmers to become Programming Managers.This is a leadership and technical role and is suitable for an experienced Principal Programmer with extensive experience leading clinical trials (phases I-IIIB) – SAS or R programmers are considered for this position.RESPONSIBILITIESFully responsible for leading multiple global projects (phases I-III), this includes but is not limited to planning and managing programming activities and QC, leading all communications and internal and external meetings, and resource and budget planning.Hands-on technical focus efficacy ADaM programming for later phase projects.Create SDTM, ADaM, and TFLs and write specifications from scratch, as well as using templates.Mentor/manage more junior members of the team.COMPANY BACKGROUNDA mid-size CRO with 1000 employees stretching across 30-40 countries. They have been around for over 25 years and so still have the stability and really are specialists in their field. They’re a rare-diseases specialist CRO with a strong oncology portfolio and so you will be working on some really interesting/complex studies across phases I-III and so will be great for your development working with this type of data, and thus when you look to move or progress this will give you a strong advantage over others who don’t have this type of experience.SKILLS NEEDED:At least 4 years of statistical programming experience working in clinical domain.Experienced leading clinical trials (phases I-III) across any therapeutic area.Strong CDISC experience – ADAM, SDTM, TFL.Experienced with mentoring junior members of the teamTITLE: Principal Statistical Programmer LOCATION: UK, RemoteSALARY: Competitive – offering salary uplift of 15% - open discussions.Interviews will be conducted in the coming weeks and so apply now to not miss out on this competitive role. Please send your CV to Max Trafford at max@peoplewithchemistry.com.Associated keywords: Programmer, SAS, R, Clinical, Trials, Phases I, Phase II, Phase III, Senior, Principal, Manager, Pharma, Pharmaceutical, CRO, Life-Science, Oncology, Respiratory, Cardiovascular, Full-service, FS, FSP, Full-Service Provider, UK, United Kingdom, Scotland, England, Wales, London, Manchester, Cambridge, Hampshire, Bristol, South, North, West, East.

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