Director Biostatistics Oncology

Meet Life Sciences; Alameda (CA); On-site; USD 187,000 - 266,000; Full time

Job summary

Meet Life Sciences is seeking a Director of Biostatistics for a confidential biotech company focusing on oncology. This role emphasizes statistical leadership across all program phases and requires extensive experience in clinical biostatistics along with a strong understanding of regulatory expectations. You'll lead vital analyses and contribute significantly to clinical programs within a mission-driven environment.

Qualifications

• Advanced degree in Biostatistics or related field.
• 8-10 years of clinical biostatistics experience.
• Knowledge of oncology trials preferred.

Responsibilities

• Lead the statistical design and analysis of clinical trials (Phases I–IV).
• Collaborate on study design and reporting.
• Oversee CROs and ensure quality standards.

Skills

CDISC standards

Statistical analysis

Clinical development

Regulatory submissions

SAS proficiency

Collaboration

Education

MS or PhD in Biostatistics

Tools

SAS

R

nQuery

EAST

Job description

2 days ago Be among the first 25 applicants

This range is provided by Meet Life Sciences. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$187,500.00/yr - $266,000.00/yr

Full-Time | Confidential Biotech Company | Therapeutic Focus: Oncology

We are partnering with an innovative biotech company that is looking to add a Director of Biostatistics to their growing clinical development team. This role will provide statistical leadership across programs and trials from early to late phase, with a strong focus on oncology and rare disease indications.

Responsibilities:

• Lead the statistical design, conduct, and analysis of clinical trials (Phases I–IV)
• Review protocols, case report forms, and statistical analysis plans
• Perform or oversee statistical analyses and interpretation of study results
• Collaborate cross-functionally on study design, data standards, and reporting
• Support integrated summaries of efficacy and safety (ISE/ISS) for regulatory submissions
• Provide statistical support during interactions with health authorities (FDA, EMA, PMDA)
• Guide development and implementation of biostatistics standards and processes
• Oversee CROs and vendor deliverables, ensuring timelines and quality are met

Qualifications:

• Advanced degree (MS or PhD) in Biostatistics or related field
• Minimum 8–10 years of experience in clinical biostatistics within biotech or pharma
• Strong knowledge of CDISC standards (SDTM, ADaM)
• Experience supporting regulatory submissions, including NDAs/BLAs
• Proficiency in SAS; familiarity with other statistical tools (e.g., R, EAST, nQuery) is a plus
• Direct experience working on oncology trials preferred
• Strong understanding of clinical development, regulatory expectations, and cross-functional collaboration

This is a high-impact role offering strategic visibility and the opportunity to contribute to meaningful clinical programs. Candidates seeking a dynamic, mission-driven environment with strong growth potential are encouraged to apply.

Please reach out to Martin Wenzel if you're interested in learning more: [e-mail]

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Staffing and Recruiting, Biotechnology Research, and Pharmaceutical Manufacturing

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