1mo
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Statistical Programmer II
United States or Atlanta or Austin or Houston or Raleigh or Phoenix or Boston or Minneapolis or Dallas
$90k-$100k/yr RemoteFull Time
Bachelor's in a quantitative field, relevant clinical trial/statistical programming experience, strong SAS skills, knowledge of SDTM/ADaM and programming QC, ability to produce validated, well-documented code and collaborate with cross-functional teams.
SAS, SAS Enterprise Guide, R, Python, SQL, Git, CDISC, SDTM, ADaM
2d
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Senior Statistical Programmer FSP
Cambridge or Spain or United Kingdom or Netherlands
RemoteFull Time
8+ YOEBachelor's in statistics/CS/math,8+ years SAS clinical trial programming experience,study lead experience,CDISC SDTM/ADaM expertise,QC/validation and submission document experience.
SAS, CDISC SDTM, ADaM, define.xml, eCRTs
4d
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Principal Statistical Programmer
Warren or Cambridge
$110k-$179k/yr OnsiteFull Time
3+ YOEMaster's degree, 3+ years programming experience, proficiency with SAS, ability to lead programming and QC for clinical study analysis datasets and TFLs.
SAS
1w
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Principal Statistical Programmer
Boston, Massachusetts, United States
$149k-$224k/yr HybridFull Time
8+ YOEB.S. in a scientific discipline, 8+ years clinical programming experience, proficiency with SAS and CDISC, eCTD submission experience, strong communication and project skills.
SAS, SAS/STAT, SAS/GRAPH, Macro, CDISC Standards, eCTD
18h
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Part-Time Contract Statistical Programmer
Lexington or United States
$114-$133/hr HybridPart Time, Contract
8+ YOE3+ MgmtGraduate degree and 8+ years statistical programming in pharma/CRO, 3+ years supervising, expert SAS, CDISC SDTM/ADaM, regulatory submission (BLA/NDA) experience, Pinnacle 21 and eCTD exposure.
SAS, R, Pinnacle 21, eCTD
1w
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Senior R Statistical Programmer
Cambridge, Massachusetts, United States
RemoteFull Time
5+ YOE5+ years industry experience; expertise in R for regulated clinical development, tidyverse data manipulation, R visualization, R package development, SAS preferred, Posit familiarity, and clinical trials data experience.
R, tidyverse, SAS, SAS/MACRO, Posit Workbench, Positron, Connect
1d
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Director, Statistical Programming
Madison or Cambridge or Princeton
$217k-$294k/yr OnsiteFull Time
10+ YOEMS (~10+ yrs) or BS (~12+ yrs) industry experience; leadership in statistical programming, clinical development knowledge, regulatory standards, talent recruitment/retention, and process transformation.
1w
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Associate Director, Statistical Programming
Boston, Massachusetts, United States
$165k-$200k/yr HybridFull Time
8+ YOEMasters in statistics/engineering or related field, minimum 8 years statistical programming/biostatistics in pharma, proficient in SAS and CDISC (ADaM/SDTM), strong regulatory knowledge and study management skills.
SAS, CDISC ADaM, CDISC SDTM
1mo
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Associate Director, Statistical Programming
Cambridge or Alaska or Arizona or Hawaii or Michigan or Tennessee
$188k-$211k/yr RemoteFull Time
6+ YOEMS in Statistics/CS (6+ years SAS pharma) or BS (8+ years); expert SAS and CDISC (SDTM/ADaM); FDA/ICH regulatory experience; R preferred; ability to lead statistical programming for clinical trials and submissions.
BASE/SAS, SAS/STAT, SAS/GRAPH, SAS MACROS, SAS, R, CDISC, SDTM, ADaM, eCTD
2w
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Senior / Principal Statistical Programmer, Clinical Development Data Services, R&D, Orion Corporation
Cambridge or Cambridge
$100k-$180k/yr HybridFull Time
5+ YOEBachelor's degree in quantitative field, 5+ years statistical programming in pharma, strong SAS skills, CDISC/define.xml and submission experience, familiarity with Pinnacle 21, ability to apply automation/AI, mentoring experience.
SAS, R, Python, Pinnacle 21, CDISC
1mo
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Associate Director, Statistical Programming
Waltham, Massachusetts, United States
$175k-$204k/yr OnsiteFull Time
10+ YOEBachelor's required (advanced degree preferred). Minimum 10 years statistical programming in pharma/biotech. Advanced SAS required; experience with R/Python, CDISC SDTM/ADaM, eCTD, regulatory submissions, vendor oversight, and leadership experience.
SAS, R, Python, CDISC SDTM, CDISC ADaM, eCTD
2w
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Statistical Programming Lead, Clinical Data Management, R&D, Orion Corporation
Cambridge or Cambridge
$130k-$230k/yr HybridFull Time
10+ YOEDegree in a quantitative discipline,10+ years statistical programming in pharma,expertise in SAS and CDISC,experience leading programming across clinical programs,and knowledge of regulatory submission standards.
SAS, Base SAS, Macro, SQL, R, Python, SDTM, ADaM, define.xml, CDISC
1w
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Senior Manager, Statistical Programming
Boston, Massachusetts, United States
$151k-$172k/yr HybridFull Time
5+ YOEMasters degree, 5+ years statistical programming/biostatistics in pharma/biotech, proficient in SAS, CDISC SDTM/ADaM, regulatory knowledge, study management and programmer oversight.
SAS, CDISC ADaM, CDISC SDTM, e-CTD
1mo
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ADS Programmer (Boston, On-Site)
Boston, Massachusetts, United States
$97k-$180k/yr OnsiteFull Time
2+ YOEBachelor's or Master's in a quantitative field; 2–4 years statistical programming (or advanced degree with 0–2); knowledge of SAS or R; experience with SDTM/ADaM and TLFs preferred; strong QC and communication skills.
SAS, R, Insight Engine, Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM), Clinical Data Interchange Standards Consortium (CDISC)
1d
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Senior Manager, Biostatistics
Boston, Massachusetts, United States
$120k-$157k/yr OnsiteFull Time
1+ YOEMSc (or equivalent) in statistics/mathematics required, 1-2 years pharmaceutical experience, competent SAS and R programmer, BPharm regulatory knowledge, strong communication and collaboration skills.
SAS, R
1mo
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Senior Statistician II - Biostatistics
Boston, Massachusetts, United States
OnsiteFull Time
3+ YOEMSc/PhD in statistics or mathematics, 3+ years pharmaceutical development experience, competent SAS and R programmer, knowledge of regulatory requirements, clinical study design/analysis/reporting, strong communication and collaboration skills.
SAS, R
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