Associate Director of Biostatistics

PRIMARY RESPONSIBILITIES:

• Direct a team of biostatisticians, taking responsibility for their individual deliverables and growth (technical and professional)
• Oversee Biostatistics contributions to oncology product clinical validation projects
• Lead development of novel statistical approaches and simulations to support innovative study designs.
• Produce, review, and standardize high-quality documentation for cross-functional internal and external collaborators and stakeholders
• Identify risks, communicate concerns, and champion solutions to cross-functional project teams
• Continuously improve the efficiency and efficacy of team through innovative techniques and strategies

QUALIFICATIONS:

• Advanced degree (Ph.D. or M.S.) in Biostatistics, Statistics, or a related quantitative field (Ph.D. preferred)
• 7+ years of experience in clinical trial biostatistics
• Strong knowledge of survival analysis, censoring, and other advanced statistical techniques relevant to oncology
• Expertise with study design innovation and power/simulation approaches
• Proven track record in mentoring and developing junior staff
• Ability to communicate complex statistical concepts clearly to both technical and non-technical audiences and foster collaborative, cross-functional partnerships

KNOWLEDGE, SKILLS, AND ABILITIES:

• Strong technical leadership and strategic thinking.
• Proven success leading and developing teams.
• Deep expertise in statistical methods for diagnostics and clinical trials, including FDA requirements.
• Effective collaborator across diverse technical disciplines.