Director, Biostatistics - Lead Innovative Clinical Trials

Bristol-Myers Squibb Co

Madison (NJ)

Presencial

USD 219 000 - 265 000

Tempo integral

Há 9 dias
Gerador de candidaturas

Uma candidatura feita para esta oferta de emprego — um currículo e uma carta de apresentação personalizados que vão ao encontro do anúncio.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Flexible Time Off
11 paid holidays
Paid vacation

Resumo da oferta

Bristol Myers Squibb Co is seeking a Director of Biostatistics to lead the statistical design and analysis for oncology, hematology, cell therapy, and related therapeutic areas. You will shape trial designs to support regulatory approvals and market access while guiding statisticians to deliver timely, high-quality results.

The role requires extensive experience in clinical trials, collaboration across cross-functional teams, and interaction with health authorities.

Qualificações

  • PhD (9+ years experience) or MS (11+ years experience) in statistics/biostatistics or related field with clinical trials experience.
  • Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis.
  • Experience in interfacing with regulatory agencies and global regulatory interactions.

Responsabilidades

  • Design innovative and efficient study designs to support regulatory approval and market access.
  • Provide statistical leadership and guidance to a biostatistical team to ensure high-quality deliverables.
  • Lead and defend statistical solutions to governance bodies and regulatory reviewers, influencing key decisions.

Conhecimentos

SAS
R
Python

Formação académica

PhD/MS in statistics/biostatistics

Ferramentas

SAS
R
Python

Descrição da oferta de emprego

Bristol Myers Squibb Co is seeking a Director of Biostatistics to lead the statistical design and analysis for oncology, hematology, cell therapy, and related therapeutic areas. You will shape trial designs to support regulatory approvals and market access while guiding statisticians to deliver timely, high-quality results.

The role requires extensive experience in clinical trials, collaboration across cross-functional teams, and interaction with health authorities.

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