Senior Clinical SAS Programmer Jobs in London, England | Glassdoor
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Senior Clinical SAS Programmer Jobs in London, England

15 Jobs

  • 3.9
    S E C Recruitment Limited – United Kingdom
    5 days ago 5d
    SeniorSASProgrammer Location: Timisoara area or home based across Romania Yearly Salary: 35,000 - 50,000 + Bonus & Benefits… leader within pharmaceutical industry is looking for a SeniorSASProgrammer on a remote basis or based in Timisoara area to join…
  • 3.0
    Worldwide Clinical Trials – London, England
    23 days ago 23d
    of clinical study data processing and reporting. Validate software, in the role of system owner or tester, and test SAS Macros… advanced SAS programming skills with expert knowledge in SAS/Macro, Proc Report and ODS. Good working knowledge in SAS/Graph, Proc…
  • 4.5
    i-Pharm Consulting Ltd – United Kingdom
    6 days ago 6d
    Are you an experienced SASProgrammer looking for an exciting new opportunity to lead projects in a leading global CRO? If so… role for you! I'm currently looking for an experienced SASprogrammer to help lead Phase IIb-III studies for a top 5 global CRO…
  • 3.4
    QuintilesIMS – London, England
    19 days ago 19d
    Excellence is a chance to revolutionize the clinical research industry. Manager / Senior Manager, Programming – the role This… creating the next generation of clinical development. Our new solutions combine world-class clinical research and data-driven insights…
  • Just Pharma – United Kingdom
    12 days ago 12d
    opportunity for a motivated Statistician/Programmer/SAS professional to join a dynamic, diverse clinical programming team in a global setting… Health Technology Assessment dossiers. - Use the SAS program to take clinical trial data from my client's global ongoing studies…
  • 1.8
    C.K. Associates Limited – United Kingdom
    8 days ago 8d
    Jenni Woolley is recruiting for a Senior Statistical Programmer to join a company in the Pharmaceutical industry at their site… Computer Science or related) - Thorough knowledge of SAS programming In order to be considered for this role, you will be required…
  • 3.4
    QuintilesIMS – London, England
    16 days ago 16d
    programming and/or clinical drug development process Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language… In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International…
  • 3.4
    QuintilesIMS – London, England
    16 days ago 16d
    programming and/or clinical drug development process Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language… In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International…
  • 3.5
    MMS Holdings Inc. – London, England
    EASY APPLY
    HOT
    Strong knowledge of and experience with SAS (SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph). Able to be in a hands-on role… appropriate analyses for clinical endpoints based on input from the protocol and the client. Performs senior-level reviews and is…
  • MSD Job Segment: Medical, Statistics, Developer, Pharmaceutical, Pro – London, England
    13 days ago 13d
    analytical field with prior SAS programming experience preferably in analysis and reporting of clinical trial projects - Excellent… The statistical programmer contributes to the definition and implementation of strategic solutions utilizing SAS to create analysis…
  • MSD – London, England
    20 days ago 20d
    analytical field with prior SAS programming experience preferably in analysis and reporting of clinical trial projects - Excellent… The statistical programmer contributes to the definition and implementation of strategic solutions utilizing SAS to create analysis…
  • Advanced Regulatory – United Kingdom
    EASY APPLY
    NEW
    co-develop regulatory strategies, have authored Brochures for EMA SA / EOP2 and or EOP3 Pre-Sub meetings or contribute to a major submission… co-author regulatory documents, with peer review, to take clinical data and clinical science and develop narratives in to strategies and…
  • Advanced Regulatory – United Kingdom
    EASY APPLY
    NEW
    co-develop regulatory strategies, have authored Brochures for EMA SA / EOP2 and or EOP3 Pre-Sub meetings or contribute to a major submission… co-author regulatory documents, with peer review, to take clinical data and clinical science and develop narratives in to strategies and…
  • Hoddesdon, East of England, England
    20 days ago 20d
    analytical field with prior SAS programming experience preferably in analysis and reporting of clinical trial projects Excellent… The statistical programmer contributes to the definition and implementation of strategic solutions utilizing SAS to create analysis…
  • 3.7
    GlaxoSmithKline – Uxbridge, England
    18 days ago 18d
    , training and performance feedback to less seniorprogrammers. Lead non-clinical projects within department or across the wider… activities. The Principal/Manager Programmer acts as a lead clinicalprogrammer for GSK clinical trials, accountable for creating…
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