Senior Biostatistician, Oncology Trials Lead

Ephicacy

United States

Presencial

USD 120 000 - 180 000

Tempo integral

Há 8 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Resumo da oferta

Ephicacy seeks a Biostatistician to provide statistical expertise for oncology clinical trial projects, ensuring accuracy, quality, and reproducibility of statistical deliverables. You will collaborate with study teams and functional partners to drive analyses and interpretation.

The role requires PhD or MSc in Statistics/Biostatistics and hands-on experience with Phase II/III oncology trials, CDISC SDTM/ADaM, and proficiency in SAS or R.

Qualificações

  • Hands-on support for oncology Phase II/III trials.
  • Strong knowledge of event-driven analyses and endpoints.
  • CDISC SDTM/ADaM expertise and clinical trial documentation.
  • Proficiency in SAS and/or R for programming and data processing.
  • Solid understanding of statistical methods and experimental design.

Responsabilidades

  • Support statistical analyses of oncology endpoints and event-driven analyses.
  • Perform event projections to estimate timelines for analyses.
  • Review SDTM/ADaM specs, TLFs, SAPs, and trial docs.
  • Identify data inconsistencies and patterns in study data reviews.
  • Validate outputs and maintain quality control documentation.
  • Collaborate with biostatistics, programming, and study teams.

Conhecimentos

Phase II/III oncology trials
Event-driven analyses
CDISC SDTM/ADaM
SAS and/or R
Statistical methodologies
Documentation & cross-functional coll.

Formação académica

PhD in Statistics/Biostatistics/related
Master’s in Statistics/Biostatistics/related

Ferramentas

SAS
R

Descrição da oferta de emprego

Ephicacy seeks a Biostatistician to provide statistical expertise for oncology clinical trial projects, ensuring accuracy, quality, and reproducibility of statistical deliverables. You will collaborate with study teams and functional partners to drive analyses and interpretation.

The role requires PhD or MSc in Statistics/Biostatistics and hands-on experience with Phase II/III oncology trials, CDISC SDTM/ADaM, and proficiency in SAS or R.

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