Biostatistics Lead, Clinical Development

Bristol Myers Squibb

Brisbane (CA)

Hybrid

USD 190,000 - 264,000

Full time

5 days ago
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Benefits offered by this job

Comprehensive benefits
Flexible time off
Stock opportunities

Job summary

Bristol Myers Squibble is seeking an Associate Director of Biostatistics to join cross-functional development teams. You will contribute to trial design, analysis planning, interpretation of results, and regulatory submissions.

With experience, you may support a specific indication and collaborate with the Biostatistics Lead and other team members. You will apply extensive knowledge of statistical methods to clinical development, lead multiple studies, and engage as a scientific partner in the

Qualifications

  • PhD with 6+ years’ experience or MS with 8+ years’ experience in statistics/biostatistics linked to clinical trials or drug development.
  • Proficiency in SAS, R or Python and advanced statistical methods.
  • Strong writing, communication, and organizational skills.
  • Expertise in statistical/clinical trials methodology for clinical development.
  • Understanding of regulatory landscape and experience with regulatory interactions.

Responsibilities

  • Design of innovative and efficient clinical trials; select populations/endpoints and contribute to strategy.
  • Defend protocols and analysis plans; independently review protocols.
  • Author/review protocol, SAP, CSRs, publications and other study documents.
  • Present data and analyses clearly and transparently.
  • Provide statistical support for health authority requests, publications, and disclosures.

Skills

Biostatistics
Statistical analysis
Interpersonal skills
Regulatory understanding
Project management

Education

PhD in statistics/biostatistics
MS in statistics/biostatistics

Tools

SAS
R
Python

Job description

Bristol Myers Squibble is seeking an Associate Director of Biostatistics to join cross-functional development teams. You will contribute to trial design, analysis planning, interpretation of results, and regulatory submissions.

With experience, you may support a specific indication and collaborate with the Biostatistics Lead and other team members. You will apply extensive knowledge of statistical methods to clinical development, lead multiple studies, and engage as a scientific partner in the

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