Lead statistical programming activities including SAS programming, SOP development, programming validation, and ensuring regulatory compliance for analysis datasets and TLFs.
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
Experience in biostatistical programming (SAS), SOP development, regulatory compliance, programming validation, and collaboration with IT to support secure statistical computing environments.
RegeneronNasdaq: REGN: Discovers and manufactures medicines for serious diseases.
10+ YOEMaster's degree and 10+ years clinical programming experience; advanced SAS (Base, Stat, Macro, Graph); project and people management; therapeutic area and regulatory submission knowledge.
Merck & Co.NYSE: MRK: Produces prescription medicines, vaccines, and animal health products.
3+ YOE3+ years SAS clinical trial programming experience; experience with CDISC/ADaM and SDTM; bachelor's in related field with 5 yrs experience or master's with 3 yrs; ability to design analysis datasets, TLFs, and lead/coordinate programming teams.
SAS, SAS/MACRO, SAS/GRAPH, CDISC Analysis Data Model (ADaM), SDTM
King of Prussia or Maidenhead or Waltham or Glattbrugg
$239k-$308k/yrOnsiteFull Time
CSLASX: CSL: Develops and manufactures biopharmaceutical products and vaccines.
10+ YOE5+ MgmtBSc in Computer Science/Math/Statistics or equivalent, 10+ years industry experience in biotech/pharma/CRO, 5+ years supervisory experience preferred, advanced SAS and CDISC knowledge, CRO management experience, strong communication and leadership skills.
Uniquity Bio: Develops novel therapeutics for immune-mediated diseases.
12+ YOE12+ years statistical programming experience in biotech/pharma/CRO, leadership experience, CDISC/SDTM/ADaM expertise, expert SAS, familiarity with R/Python, experience with regulatory submissions and CRO/vendor management.
7+ YOE7+ years statistical programming experience (Sr Manager) or 9+ years (Associate Director) in biotech/pharma/CRO; advanced SAS proficiency, CDISC (SDTM/ADaM/Define.xml) expertise, experience with regulatory submissions, vendor/CRO oversight, and leadership/mentorship experience.
Principal / Associate Director, Statistical Programming
Conshohocken, Pennsylvania, United States
$180k-$219k/yrOnsiteFull Time
Madrigal PharmaceuticalsNASDAQ: MDGL: Develops and commercializes therapeutics for metabolic dysfunction-associated steatohepatitis.
10+ YOEBachelor's in a quantitative or life science field (Master's preferred), 10+ years pharmaceutical/biotech statistical programming with regulatory submission experience, strong SAS (macros) skills, R preferred, CDISC SDTM/ADaM expertise, and CRO oversight experience.
Everest Clinical Research: Full-service contract research organization for clinical drug development.
10+ YOEAdvanced degree in statistics or related field; extensive SAS programming experience; expertise in SDTM/ADaM; leadership in programming projects; experience with regulatory submissions.
Associate, Lines of Defense – Early Career Development Program
Newark, Delaware, United States
HybridFull Time
Sallie MaeNASDAQ: SLM: Provides private student loans and personal banking products.
Early-career program for students graduating Dec 2026–Jun 2027; degree in business, finance, data, or related field; experience with SQL, Python, SAS; analytical, communication, and collaboration skills.
American Bible Society: Translates and publishes Bibles and religious educational materials.
Manage mixed-methods research and program evaluations, analyze data with SPSS/SAS, use Qualtrics and Tableau, publish research, and communicate findings to stakeholders.
SPSS, SAS, Qualtrics, Tableau Desktop, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Otsuka PharmaceuticalTokyo Stock Exchange: 4578: Develops and manufactures innovative pharmaceutical and nutritional products.
12+ YOE5+ MgmtPhD in Statistics or Biostatistics; 12+ years in pharma/biotech; 5+ years of people leadership; deep clinical development knowledge; strong SAS/programming skills.
Senior Government Consultant - Program/Waiver Evaluation & Implementation Specialist
Phoenix or Boston or Hartford or Philadelphia or Milwaukee or Washington or Seattle or Chicago or Dallas or Minneapolis or Atlanta
$88k-$176k/yrHybridFull Time
Marsh McLennanNYSE: MRSH: Global professional services firm providing risk, strategy, and people solutions.
3+ YOEMaster's degree or higher, minimum 3 years' experience evaluating Medicaid programs, expertise in research design and statistical analysis, knowledge of Medicaid policy, SAS experience preferred, strong communication and project management skills.
TransamericaNYSE: AEG: Provides insurance, retirement solutions, and investment products to customers.
2+ YOEBachelor's in a quantitative discipline, modeling and analytics experience, 2+ years programming (C++, C#, Python), familiarity with SAS/R/SPSS, strong finance and problem-solving skills.
Temple University: Public university providing higher education, academic research, and healthcare
3+ YOEMaster's in biostatistics/statistics (or related) plus ≥3 years statistical analysis/programming in medical research using SAS or Stata; strong communication, project management, and database skills.
SAS, Stata, Microsoft Office, SQL, EPIC, REDCap, R, Microsoft Access
Postdoctoral Research Associate in Pharmacoepidemiology
New Brunswick, New Jersey, United States
$80k/yrOnsiteFull Time
Rutgers University: Providing higher education degrees and conducting academic research.
Doctorate in a related field required; experience with pharmacoepidemiology, medical device research, EHR- and claims-based research, and programming in SAS or R; strong communication and project management skills.
Credit Model Development Quantitative Analyst I- HELOC & Residential Mortgage (Hybrid - see description for potential locations)
Buffalo or Washington or Baltimore or Iselin or Wilmington or New York City or Bridgeport
$62k-$104k/yrHybridFull Time
M&T BankNYSE: MTB: Provides retail, commercial, and institutional banking and trust services.
1+ YOEBachelor's (or equivalent) and 1+ years quantitative or data experience; SQL and statistical programming (SAS, Stata, R, Python); econometric/statistical techniques; strong communication and data visualization skills.
6+ YOE6–8+ years statistical programming for clinical trials with CDISC SDTM/ADaM expertise, Master's (or PhD) in biostatistics/statistics, SAS and Pinnacle 21 experience, regulatory submission knowledge.