6 statistical programmer jobs at 5 companies in Stamford, CT
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Senior Statistical Programmer
Franklin Lakes, New Jersey, United States
$110k-$176k/yr OnsiteFull Time
3+ YOE3+ years statistical programming experience (SAS or R), Bachelor's in Statistics/CS/Life Sciences required, strong regulatory clinical trials knowledge (GCP/ICH), validation and QC experience, strong communication and problem-solving.
R, SAS
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Statistical Clinical Programmer
Ridgefield, Connecticut, United States
$115k-$181k/yr OnsiteFull Time
3+ YOEBachelor's degree with 3+ years of data science experience or related master's degree; clinical research, statistical methodology, R, clinical trials, CDISC, and English fluency required.
R, Clinical Data Interchange Standards Consortium (CDISC)
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Senior Statistical Programmer
North Wales or Rahway
$117k-$184k/yr HybridFull Time
3+ YOEBA/BS plus 5–9 years SAS/R clinical trial programming experience or MS plus 3–7 years; experience with CDISC (SDTM/ADaM), complex data manipulation, and regulatory submission programming.
SAS, R, Python, NonMem, CDISC SDTM, ADaM
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Assoc Director, Statistical Programming
East Hanover, New Jersey, United States
$146k-$270k/yr OnsiteFull Time
University degree in life science/computer science/data science/pharmacy/statistics/nursing; proven leadership in statistical programming for clinical trials; knowledge of clinical trial methodology and GCP; ability to manage resources, ensure quality, and collaborate cross-functionally.
R, Tidyverse, R Shiny, Git
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Assoc Director, Statistical Programming
East Hanover, New Jersey, United States
$146k-$270k/yr HybridFull Time
University degree in life/data science or related, proven leadership and statistical programming experience in clinical trials, knowledge of GCP, ability to manage teams, and strong communication and problem-solving skills.
Tidyverse, R, R Shiny, Git
2mo
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Associate Director Statistical Programming - Pharmacometrics
Tarrytown or Warren
$176k-$287k/yr HybridFull Time
10+ YOEMaster's in a quantitative field,10+ years programming experience in clinical trial data,expert SAS skills,CDISC knowledge,biostatistics/pharmacometrics understanding,project and people management experience.
SAS, SAS Studio, Microsoft Excel, R, Python, CDISC