Associate Director, Biostatistics

BeiGene

California, US
Base: $162,600.00 - $212,600.00 annually; bonus/eq...
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Phd in statistics or related field
4+ years clinical drug development experience
Sas and/or r programming knowledge
** BeiGene is seeking an Associate Director of Biostatistics to lead and support the statistical aspects of clinical trials. The ideal candidate should possess a PhD or Master's degree with substantial experience in clinical drug development, preferably with knowledge of oncology. **

Job Summary

  • The role involves serving as a statistical lead in cross-functional teams to ensure study designs meet program objectives and regulatory needs.
  • Candidates will independently apply complex statistical techniques to analyze clinical trial data and prepare reports for regulatory agencies.
  • BeOne offers a comprehensive benefits package including medical, dental, vision, 401(k), and discretionary equity awards.

Matching Summary

Match Score: 75

** BeiGene is seeking an Associate Director of Biostatistics to lead and support the statistical aspects of clinical trials. The ideal candidate should possess a PhD or Master's degree with substantial experience in clinical drug development, preferably with knowledge of oncology. **

Salary

Base: $162,600.00 - $212,600.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, PTO, Wellness

Skills & Requirements

Must-have

  • PhD in Statistics or related field
  • 4+ years clinical drug development experience
  • SAS and/or R programming knowledge
  • Clinical trial design and execution expertise
  • Regulatory guidance knowledge

Nice-to-have

  • Oncology experience preferred
  • Innovative statistical methods research
  • Strong written and oral communication skills
  • Collaborative team player with independent initiative
  • Strategic working relationship building

Key Requirements

  • Minimum PhD in Statistics or Master's with 6+ years experience
  • Demonstrated experience with clinical trials
  • Knowledge of worldwide regulatory guidance
  • Ability to work remotely near CA, MA, MD, or NJ offices

Work Rights

Not specified

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