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Clinical SAS programmer (onsite Cambridge, MA) (Science & Biotech)
Cambridge, MA 02139
Recruited by: Ali Henderson | Senior Recruiter | SimulStat Inc. See all my Jobs

  • Hiring Company: SimulStat's client
  • Industry: Science & Biotech
  • Compensation: To Be Determined
  • Expires: Sep 03, 2019
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Job Description

Senior Statistical Programmer

6 month renewable contract

Key Responsibilities

Writing SAS programs from instructions provided by Biostatisticians and Statistical Programmers to create CDISC data sets, tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications
Utilize SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH
Create all files, documents, and analyses necessary to support an electronic submissions in eCTD format, including ISS/ISE
Work with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry
Work in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards
Perform quality control checks of SAS code and output produced by other Statistical Programmers


Minimum Qualifications

Bachelor's degree in Biostatistics, Statistics, Computer Science, or a related field
5 years of SAS and relevant pharmaceutical industry experience, including CDISC SDTM and ADaM models