Sr. Statistical Programmer at Vertex in Boston, MA

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Job Description:

Position will function independently to provide statistical programming technical leadership to support team members; independently design and code complex SAS programs for applications designed to analyze and report complex clinical trial data for electronic submissions of data in CDISC format; provide guidance on the resolution of highly complex clinical trial reporting problems within budget and time line constraints while assuring high quality standards; perform quality control checks of advanced SAS code and output produced by other statistical programmers; maintain working knowledge of medical data, the design and phases of clinical trials, statistics, relevant regulatory requirements, and the pharmaceutical industry; identify problems and develop global tools to increase efficiency and capacity of the statistical programming group; conduct briefings and participate in technical meetings for internal and external stakeholders; manage project timelines and schedules of specific phases of projects and contracts with internal personnel and outside stakeholders.


Master's degree (or foreign equivalent) in Biostatistics, Statistics, Natural Sciences, or another similarly quantitative analytical field and two (2) years of post-baccalaureate work experience in the job offered, as a Statistical Programmer, or in a related field. Experience must include the following: Demonstrable experience writing SAS programs to create data sets, tables, figures, and listings and reporting results of clinical trials for investigational medications; Demonstrable experience creating all files, documents, and analyses necessary to support an electronic submissions in eCTD format; Demonstrable experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH; Demonstrable experience with CDISC SDTM and ADaM models and transforming raw data into these standards; Demonstrable experience performing quality control checks of SAS code and output produced by other Statistical Programmers; Demonstrable knowledge of GCP and clinical trials; Demonstrable experience leading statistical programming activities, managing study timeline and resources, and coordinating study activities with other functions.

Send Resume to Shannon Holt at Reference 12140.195

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