Director, Biostatistics

Bicara TherapeuticsBoston, MA
$236,000 - $274,000

About The Position

Bicara is seeking an experienced Director of Biostatistics to lead statistical activities supporting our oncology clinical programs. This individual will provide both strategic direction and hands-on expertise, shaping study design, data analysis, and evidence generation across the development. In this highly visible role within a growing biotech organization, the Director will collaborate closely with internal teams and external partners to deliver high-quality, data-driven insights that advance our oncology pipeline. The ideal candidate thrives in a dynamic, fast-paced environment and is eager to contribute both technically and strategically to program success.

Requirements

  • Master’s degree or PhD in Biostatistics, Statistics, or a related quantitative field.
  • 10+ years of industry experience, including 5+ years in oncology clinical development.
  • Demonstrated hands-on experience in designing and analyzing oncology trials (e.g., dose escalation, expansion cohorts, or registrational studies).
  • Strong and proficient programming skill in SAS and/or R; working knowledge of CDISC standards (ADaM, SDTM).
  • Strong problem-solving, communication, and organizational skills.
  • Ability to work independently in a fast-paced environment.
  • Experience managing CROs and collaborating in a cross-functional matrix team.

Nice To Haves

  • Prior experience supporting regulatory submissions and interactions is preferred.

Responsibilities

  • Serve as the lead statistician for assigned oncology programs and studies.
  • Partner cross-functionally with Clinical, Regulatory, Medical, Statistical Programming, and Data Management teams to define and execute statistical strategies aligned with development objectives.
  • Provide statistical input to clinical protocols, SAPs, CRFs, and data management plans; oversee execution of analyses and reporting deliverables.
  • Perform or oversee statistical analyses using SAS and/or R, ensuring scientific rigor and reproducibility.
  • Manage and oversee deliverables from CROs and external vendors, providing statistical review, feedback, and quality control.
  • Contributes to the design and implementation of innovative statistical methodologies to enhance the efficiency and interpretability of oncology studies.
  • Promote statistical literacy across cross-functional teams, helping colleagues understand key concepts and data-driven insights.
  • Support the development of publications, abstracts, and presentations through data interpretation and statistical input.
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