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Manager Statistical Programming

Job in Lakewood, Ocean County, New Jersey, 08701, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-07-10
Job specializations:
  • IT/Tech
    Data Analyst, Data Scientist, Data Science Manager, Data Engineering
Salary/Wage Range or Industry Benchmark: 100000 - 130000 USD Yearly USD 100000.00 130000.00 YEAR
Job Description & How to Apply Below

Manager Statistical Programming Responsibilities

  • Provide timely support to the study team on all statistical programming matters according to project strategies.
  • Provide project leadership and programming support for processing data from clinical studies; guide implementation and execution of programming and project standards.
  • Lead programming for all programming deliverables through regulatory approval, product launch, data monitoring boards, and annual reports (internal or CROs).
  • Oversee documentation and ensure consistent maintenance of code, logs, and output in a regulated environment; respond to senior‑management statistical ad hoc requests.
  • Develop expertise in a therapeutic area or standard tool; work with minimal supervision to prepare, execute, report, and document projects.
  • Serve as lead programmer for development and QC of tables, listings, graphs, or systems using Regeneron tools/methodologies and CDISC SDTM/ADaM standards.
  • Manage programming effort using tools to track, allocate, and summarize work progress and completion; support complex presentations and ad hoc requests.
  • Act as programming representative in multidisciplinary study teams to support analysis and clinical trial reporting up to regulatory approval and annual reports.
  • If applicable, lead application development and represent programming to the user audience.
  • Work with management on resource requirements; review/select candidates and interview for contractor and permanent positions.
  • Provide feedback on team contributions and recommend yearly goals; advise direct reports on retention of data, records, and information procedures.
Qualifications
  • Master’s Degree.
  • 8–10 years of relevant work experience.
  • SAS Certification desirable.
  • Alternatively: 5+ years programming experience processing clinical trial data in biotech/pharma/health industries, with some project and people management experience and a Master’s in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline.
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