Director of Biostatistics

Eupraxia Pharmaceuticals

$225K — $260K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree or PhD in biostatistics or statistics
  • 15+ years of experience in biotech/pharma as a biostatistician
  • Experience in supporting pivotal and registrational clinical trials
  • Strong oversight experience with CROs and vendors
  • Proven ability to deliver high quality statistical outputs
  • Prior experience with NDA/BLA submissions

Responsibilities

  • Lead biostatistical strategy for clinical development programs
  • Contribute to study design and protocol development
  • Develop statistical analysis plans and TLF shells
  • Ensure robust clinical trial design and regulatory compliance
  • Oversee quality and timeliness of TLF production
  • Provide oversight to CROs and external statistical reporting groups
  • Manage statistical vendors for independent data monitoring committees

Benefits

  • Leader in strategic biostatistics within critical development programs
  • Opportunity to shape regulatory submissions and standards
  • Role may include mentorship of junior biostatisticians
  • Hands-on involvement with high-profile projects
  • Being part of cross-functional teams enhances collaboration and influence
Full Job Description
Scope

The Director of Biostatistics provides strategic and operational leadership for biostatistical activities within and across clinical development programs. This role is responsible for ensuring the integrity, quality, and rigor of statistical analyses and methodologies applied to clinical studies. They will serve as the primary statistical representative in cross-functional teams and lead biometrics related activities for regulatory submissions (IND, NDA/BLA, MAA). This role may supervise junior statisticians or function as a senior individual contributor.

Reports to: VP of Biometrics and Data Management

Key responsibilities and duties:
  • Leads and oversee biostatistical strategy for one or more clinical development programs.
  • Serves as a key contributor to study design and protocol development.
  • Develops statistical analysis plans (SAPs) and table, listing, and figure (TLFs) shells.
  • Ensures that clinical trial designs and proposed analysis methods are robust and follow regulatory guidelines (FDA, EMA, etc.)
  • Oversees the production of TLFs for interim and final analyses and ensures that it is of high quality and delivered on time.
  • Provides hands-on oversight of CROs and external statistical reporting groups to ensure quality standards and timelines are met for statistics related deliverables
  • Manages statistical vendors for independent data monitoring committees
  • May supervise junior biostatisticians


Education, qualifications and work experience:
  • Master's degree or PhD in biostatistics or statistics
  • 15+ years of biotech/pharma experience as a biostatistician
  • Demonstrated experience supporting pivotal and registrational clinical trials
  • Strong CRO and vendor oversight experience
  • Track record of delivering high quality statistical related deliverables
  • NDA/BLA experience


Additional attributes:
  • Excellent knowledge of SAS
  • Experience with sample size calculation software such as nQuery, EAST, etc.
  • Knowledge of R a plus


Salary Range: $225,000 to $260,000 depending on education and relevant work experience

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