Biostatistics Director, Clinical Strategy (Remote)

Immunovant

New York (NY)

On-site

USD 270,000 - 310,000

Full time

14 days+
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Benefits offered by this job

Equity
Medical, dental, vision
401k
Unlimited paid time off
Parental leave

Job summary

Immunovant, Inc. is seeking a Senior Director of Biostatistics to lead the statistics strategy across multiple development programs. You will collaborate with internal and external stakeholders to execute the Biostatistics plan in a fast-paced biotech environment.

The role requires a PhD in statistics/biostatistics and 12+ years of biotech/pharma experience, with strong regulatory engagement and mathematical expertise guiding translational decisions and submissions.

Qualifications

  • PhD in statistics/biostatistics or related field.
  • 12+ years of experience in biotechnology, pharmaceutical or health-related area.
  • Knowledge of Health Authority guidelines and ICH regulations.
  • Experience engaging with Health Authorities.
  • Deep understanding of drug development from Phase 2 to launch.
  • Ability to collaborate with diverse stakeholders.
  • Strong written and oral communication skills.

Responsibilities

  • Oversee statistics strategy, planning, execution, and communication for assigned programs.
  • Provide input on clinical development plans, SAPs, regulatory submissions and questions.
  • Collaborate with clinical teams and partner lines (e.g., Medical Directors, Regulatory).
  • Ensure study and project statistics activities comply with regulatory requirements and company standards.
  • Identify opportunities to apply innovative statistical methods to streamline development.
  • Manage indication/study biostatisticians.

Skills

Leadership in Biostatistics
Regulatory engagement
Cross-functional collaboration
Statistical methodology

Education

PhD in Statistics/Biostatistics/Mathematics or related field

Job description

Immunovant, Inc. is seeking a Senior Director of Biostatistics to lead the statistics strategy across multiple development programs. You will collaborate with internal and external stakeholders to execute the Biostatistics plan in a fast-paced biotech environment.

The role requires a PhD in statistics/biostatistics and 12+ years of biotech/pharma experience, with strong regulatory engagement and mathematical expertise guiding translational decisions and submissions.

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