VP, Biometrics

AbCellera Biologics Inc.

San Francisco (CA)

On-site

USD 300,000 - 500,000

Full time

14 days+

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Job summary

Scorpion Therapeutics is seeking a Strategic VP of Biometrics to lead biostatistics, programming, analysis, and clinical data management across the full pipeline from IND-enabling studies to post-approval. The role reports to the Chief Medical Officer and focuses on building high-performing teams and shaping data strategy.

Responsibilities span study design, regulatory interactions for Phase 1–4 trials, and collaboration with cross-functional teams and external vendors, with strict adherence to

Qualifications

  • 15+ years biotech/pharma leadership with 12+ years in biostatistics.
  • Extensive experience with NDA/BLA submissions.
  • Advanced degree in biostatistics or related field; expert knowledge ICH, GCP, CDISC; proven leadership.

Responsibilities

  • Build and oversee high-performing biometrics teams.
  • Shape clinical data strategies across programs.
  • Design studies within Phase 1-4.
  • Lead regulatory interactions for submissions.
  • Partner with cross-functional teams and external vendors.
  • Ensure compliance with GCP, ICH, and CDISC standards.
  • Advise on quantitative methodologies for regulatory submissions.

Skills

Biostatistics leadership
Regulatory submissions (NDA/BLA)
ICH/GCP/CDISC knowledge
Team leadership
Data strategy

Education

Advanced degree in Biostatistics or related field

Tools

CDISC standards knowledge
GCP knowledge
ICH guidelines knowledge

Job description

Role

Strategic VP, Biometrics leading biostatistics, statistical programming, analysis, and clinical data management across the full pipeline from IND-enabling studies to post-approval.

Responsibilities
  • build and oversee high-performing teams
  • shape clinical data strategies
  • study designs
  • regulatory interactions for Phase 1-4 trials
  • partner with cross-functional teams and external vendors
  • ensure compliance with GCP, ICH, and CDISC standards
  • advise on quantitative methodologies for regulatory submissions
Requirements

15+ years biotech/pharma leadership with 12+ years in biostatistics, extensive experience with NDAs/BLA submissions, advanced degree in biostatistics or related field, expert knowledge of ICH, GCP, CDISC; proven talent leadership.

HighValue

clinical-stage biotech developing antibody-based medicines across endocrinology, women’s health, immunology, oncology; pipeline includes multiple drugs in clinical and preclinical phases, with emphasis on regulatory interactions and data strategy.

WorkSetup

senior leadership role, reporting to Chief Medical Officer, with a focus on collaboration and strategic oversight.

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