Oncology Lead Biostatistician – Late-Phase

Redbock - an NES Fircroft company

San Francisco (CA)

Vor Ort

USD 150.000 - 210.000

Vollzeit

Vor 11 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Redbock - an NES Fircroft company in San Francisco seeks a lead or supporting statistician for late-phase oncology studies. You will coordinate with cross-functional teams to ensure timely, high-quality deliverables and work on design, analysis and reporting of clinical studies.

PhD or MS in statistics/biostatistics with 5–8 years biotech/pharma experience required, with solid tumor late-stage drug development.

Qualifikationen

  • PhD or MS in statistics/biostatistics with biotech/pharma experience.
  • Experience with oncology late-phase studies preferred.
  • Familiarity with NDA/BLA submissions desirable.

Aufgaben

  • Provide statistical expertise in design, analysis and reporting of clinical studies.
  • Partner with cross-functional teams to define analysis scope and timeline.
  • Develop statistical analysis plans and detailed analysis specifications.
  • QC statistical analyses and perform necessary modeling.
  • Collaborate with statistical programmers to ensure analyses follow the plan.
  • Coordinate with Data Management and Clinical Operations for robust data collection.
  • Contribute to publications ensuring data consistency.
  • Prepare statistics sections for Health Authority submissions.
  • Represent biostatistics on study teams and support cross-functional decisions.

Kenntnisse

Statistical analysis
Cross-functional collaboration
Clinical study design

Ausbildung

PhD or MS in statistics/biostatistics

Tools

SAS
R

Jobbeschreibung

Redbock - an NES Fircroft company in San Francisco seeks a lead or supporting statistician for late-phase oncology studies. You will coordinate with cross-functional teams to ensure timely, high-quality deliverables and work on design, analysis and reporting of clinical studies.

PhD or MS in statistics/biostatistics with 5–8 years biotech/pharma experience required, with solid tumor late-stage drug development.

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