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.

Qualification:

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 Shannon_Holt@vrtx.com. Reference 12140.195

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