Biostatistics Program Lead — Remote (Phase I–IV)

Oruka Therapeutics Inc

Boston (MA)

Híbrido

USD 182 000 - 208 000

Tempo integral

Há 5 dias
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Currículo e carta de apresentação personalizados, prontos a enviar.

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Vantagens oferecidas por esta oferta de emprego

Competitive salary
Equity potential
Professional growth
Inclusive culture

Resumo da oferta

Oruka Therapeutics Inc. is seeking an Associate Director, Biostatistics to lead statistical leadership for multiple clinical programs from Phase I to IV.

You will design studies, develop SAPs, and guide reporting and interpretation of results in a fast-paced biotech setting. The role requires strong expertise in biostatistics, trial design, and statistical programming (SAS, R), with the ability to manage CRO vendors and work across functions.

Qualificações

  • PhD in Biostatistics or related field with 5+ years in clinical trials (or a Master with 8+ years).
  • Expertise in trial design, sample size, modeling, and analysis.
  • Ability to lead cross-functional teams and provide independent statistical judgment.

Responsabilidades

  • Lead statistical design for assigned programs and provide input on study design and SAPs.
  • Oversee timelines and deliverables for biostatistics across projects.
  • Prepare and review statistical sections of protocols and reports with independence.
  • Coordinate data management and programming deliverables to align with analysis plans.
  • Oversee CRO biostatistics vendors and ensure timely, quality outputs.

Conhecimentos

Statistical leadership
Cross-functional leadership
Biostatistics expertise
SAS programming
R programming
Clinical trial design

Formação académica

PhD in Biostatistics
Masters with 8+ years

Ferramentas

SAS
R

Descrição da oferta de emprego

Oruka Therapeutics Inc. is seeking an Associate Director, Biostatistics to lead statistical leadership for multiple clinical programs from Phase I to IV.

You will design studies, develop SAPs, and guide reporting and interpretation of results in a fast-paced biotech setting. The role requires strong expertise in biostatistics, trial design, and statistical programming (SAS, R), with the ability to manage CRO vendors and work across functions.

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