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Senior Manager, Biostatistics

Gilead Sciences · Parsippany, NJ +1 more

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BiometricsFull-time$154k–$199kCompany career page

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Role summary

Gilead Sciences seeks a Senior Manager in Biostatistics to lead statistical analyses on clinical studies and regulatory submissions. The role involves directing internal and external teams, providing biostatistical consultation on trial design, and managing projects of increasing complexity across molecules and marketed products.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

  • PhD in biostatistics or related field with 4+ years of biomedical statistical analysis experience using SAS
  • MS in biostatistics with 6+ years of relevant experience in biomedical data analysis and SAS software
  • BA/BS in biostatistics with 8+ years of statistical analysis experience in biomedical settings
  • Proven experience leading small project teams and managing biostatistics projects effectively
  • Advanced knowledge of statistical principles, standards, and biostatistics software tools
  • Ability to learn quickly, adapt to change, and work across multiple concurrent projects
  • Experience developing software and analytical tools for biomedical statistical support

What you'll be doing

  • Lead statistical analyses and data reviews for NDA submissions in collaboration with cross-functional partners
  • Author statistical analysis plans and provide consultation on clinical trial design and study endpoints
  • Direct internal and external teams in defining, executing, and completing statistical activities for clinical trials
  • Oversee technical and operational statistical work for multiple clinical studies of increasing complexity
  • Review safety data, biomarker analyses, and clinical trial monitoring results using advanced statistical methods

Privacy & handoff

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Date posted1 day ago
Last source check1 day ago
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