Lead Statistical Programmer — AI-Driven Clinical Data Leader

Biopharma Careers

Durham (NC)

On-site

USD 130,000 - 180,000

Full time

14 days+
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Job summary

ViiV Healthcare seeks a Principal Statistical Programmer to lead programming activities for multiple clinical studies, ensuring high-quality development, validation, and delivery of complex analyses. The role drives technical excellence, regulatory compliance, and data-driven strategy, while mentoring junior staff and shaping study design.

Responsibilities include leading programming packages, adopting modern tools, and supporting QA, CDISC standards, and TMF governance.

Qualifications

  • Bachelor’s degree in Statistics, Computer Science, or a related field.
  • Expertise in R programming.
  • 6+ years of clinical programming experience.
  • 5+ years of experience in the Pharmaceutical or Biotechnology industry.
  • Experience using generative AI tools and coding assistants (e.g., GitHub Copilot, Codex, and Claude) to improve programming efficiency, automation, code quality, and analytical workflows in clinical programming.

Responsibilities

  • Lead programming for studies, ensuring efficient development and validation of analysis packages.
  • Identify and implement improvements, including use of AI/ML.
  • Maintain governance and oversee TMF compliance.
  • Communicate technical concepts, risks, and timelines clearly to stakeholders.
  • Mentor junior programmers and share best practices internally and externally.
  • Support sprint planning and project delivery across studies.
  • Collaborate cross-functionally and manage data access appropriately.
  • Provide technical input on programming strategies and study design.

Skills

R programming
Clinical programming
CDISC knowledge
AI in programming

Education

Bachelor’s degree in Statistics or related field

Tools

Git-based workflows
Open-source analytics tools

Job description

ViiV Healthcare seeks a Principal Statistical Programmer to lead programming activities for multiple clinical studies, ensuring high-quality development, validation, and delivery of complex analyses. The role drives technical excellence, regulatory compliance, and data-driven strategy, while mentoring junior staff and shaping study design.

Responsibilities include leading programming packages, adopting modern tools, and supporting QA, CDISC standards, and TMF governance.

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