Sr Statistical Programmer - Houston, TX
A client of ours in Houston, TX is seeking a Sr. Statistical Programmer.
They are a pharmaceutical company that discovers, develops and
commercializes small molecule drugs aimed at cardiovascular and inflammatory
diseases.
Major responsibilities:
Develop, standardize, and maintain SAS Macros/programs and report tools for
statistical outputs (tables, listings, and figures), and analyses of
demographic data, adverse events, and laboratory data
Oversee and coordinate statistical programming activities with outside
contractors
Perform statistical programming and validation
Collaborate with data management group to ensure data security with regard
to data extraction, transfer, and storage
Set up and maintain secure and efficient statistical programming environment
and system
Collaborate with clinical group on data review and cleaning
Assist with statistical quality control and assurance
Ensure proper documentation of statistical programs, analysis datasets, and
outputs.
Qualifications:
B.S. or M.S. in statistics, biostatistics, or related field
At least 5 years of SAS programming experience in the pharmaceutical/CRO
clinical trial (Phases I-IV) environment
Proficient in SAS programming, including SAS Macro language, SAS/Base,
SAS/STAT, and SAS/Graph
Good understanding clinical trial practices, procedures, and methodologies
Detail oriented, highly motivated, and work independently
Good verbal and written communication skills
At least three year experience in analyzing clinical trial data for Phase I,
II, III, and IV.
Very strong capability in SAS macros, especially in developing Macros for
report.
Statistics or Biostatistics degree is preferred.
Apply:
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Referrals:
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referring a colleague or friend. We do have a generous referral program.
More details are available here:
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