Stevenage - Principal Programmer/Analyst

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Bachelor’s degree with 5 to 8 years applicable experience working in a clinical trial environment. •Recognized expertise in SAS programming and SAS macro code development.  Understanding of other SAS products (e.g. SAS/GRAPH, SAS Output Delivery System)•Solid level of understanding of the pharmaceutical regulatory and publishing processes (e.g. 21 CFR Part 11)•Solid level of understanding and experience with CDISC data and standards, primarily with creating and using ADaM datasets•Previous successful direct interaction with clinical study team members•Demonstrated knowledge of basic computer skills (MS Word, Excel, PowerPoint, Outlook)•Effective verbal and written communication skills Preferred qualifications: Graduate degree •Knowledge of non-SAS programming packages/languages (e.g. Spotfire, S-Plus, R)•Ability to work simultaneously on multiple studies•Ability to manage conflicting demands and priorities and to negotiate successfully•Project management certification or relevant experience•Demonstrated ability to manage the outsourcing or externalization of statistical programming  work in the clinical trails setting (e.g., working with CROs, academic institutions)•Familiarity with the Immuno-Inflamation, Respiratory, Infectious Diseases, or Neurosciences therapeutic areas, or …

Stevenage - Pharmaceutical - Manager - GlaxoSmithKline