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Sr. Scientist, Stat. Programming, Late-Stage Oncology; Hybrid

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-08-30
Job specializations:
  • IT/Tech
    Data Analyst, Data Scientist, Data Engineering
Salary/Wage Range or Industry Benchmark: 120000 - 160000 USD Yearly USD 120000.00 160000.00 YEAR
Job Description & How to Apply Below
Position: Sr. Scientist, Stat. Programming, Late-Stage Oncology (Hybrid)

Position Supports statistical programming for late-stage drug/vaccine clinical development. May include leadership of one or more projects. Accountable for development/execution of statistical analysis and reporting deliverables (safety/efficacy datasets, tables, listings, figures) from clinical trials through worldwide regulatory submissions and post-marketing support. Designs and maintains statistical datasets supporting multiple stakeholder groups; collaborates with statistics and project stakeholders; serves as statistical programming point of contact and knowledge holder through product lifecycle.

Primary

Activities:
  • Develop and validate analysis and report programming using global/TA standards and departmental SOPs
  • Maintain and manage project plan including resource forecasting
  • Coordinate global programming team (including outsource providers)
  • Participate in departmental strategic initiative teams
Education/Minimum:
  • BA/BS in CS, Statistics, Applied Math, Life Sciences, Engineering (or related) + 5+ years SAS programming in clinical trials
  • OR
  • MS in same fields (or related) + 3+ years SAS programming in clinical trials
Required Skills/

Experience:
  • Interpersonal collaboration and negotiation; strong written/oral/presentation skills
  • Experience developing R&D analysis/reporting deliverables (data, analyses, tables, graphics, listings)
  • Project leadership; independent at project level; collaborate with stakeholders
  • Deep SAS clinical trial programming expertise (data steps, procedures, SAS/MACRO, SAS/GRAPH; systems/DB)
  • Design/develop complex programming algorithms; understand statistical terminology/concepts
  • Familiarity with clinical data management; experience with CDISC and ADaM
  • Ensure process compliance and deliverable quality; strategic-to-tactical thinking
  • Anticipate stakeholder requirements
Preferred:
  • GenAI tools (Python, R, R Shiny, etc.); reporting/SOP and SDLC knowledge
  • Regulatory submission experience (US/worldwide) incl. electronic submission deliverables
  • Programming consistency across protocols; mentor experience; cross-culture/geography experience
  • Project planning with Microsoft Project or similar; professional society activity; process improvement
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