Associate Director, Biostatistics

J&J FAMILY OF COMPANIES

Allschwil, Basel-Country, Switzerland
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Advanced statistical methodology application
Proficient in sas or r programming
Cross-functional team collaboration
** Johnson & Johnson is seeking an Associate Director of Biostatistics to provide leadership in the analysis, design, execution, and reporting of data evidence for projects. The role emphasizes innovation in statistical approaches and collaboration across departments, requiring a strong background in biostatistics and drug development. **

Job Summary

  • Johnson & Johnson provides an inclusive work environment respecting diversity and dignity of employees worldwide.
  • The role involves leading biostatistics efforts for program plans, supporting business-critical and regulatory questions with innovative statistical approaches.
  • The position represents Statistics & Decision Sciences in cross-functional teams and senior management reviews, promoting collaboration and scientific communication.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking an Associate Director of Biostatistics to provide leadership in the analysis, design, execution, and reporting of data evidence for projects. The role emphasizes innovation in statistical approaches and collaboration across departments, requiring a strong background in biostatistics and drug development. **

Skills & Requirements

Must-have

  • Advanced statistical methodology application
  • Proficient in SAS or R programming
  • Cross-functional team collaboration
  • Regulatory and decision-making support
  • Clinical trial design optimization
  • Data integrity and quality compliance

Nice-to-have

  • Innovative statistical approach implementation
  • Building cross-functional partnerships
  • Promoting diversity, equity, and inclusion
  • Strong interpersonal communication skills
  • Experience with real-world evidence (RWE)
  • Ability to adapt to changing environments

Key Requirements

  • Ph.D. in Statistics or related field with minimum 6 years experience
  • Master’s degree with commensurate experience
  • Excellent written, oral, and interpersonal communication skills
  • Understanding of drug development and regulatory acceptability
  • Ability to work independently and in interdisciplinary contexts

Work Rights

Not specified

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