Principal Statistical Programmer

critical outputs and technical documents (e.g., cSDRG, ADRG). Maintain governance and oversee TMF compliance. Drive adoption of modern technologies, standards, and Agile practices. Provide technical input on programming strategies and study design. Act as SME for emerging tools when needed. 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. Support regulatory interactions and contribute to CoE activities. Accountabilities Serve as Lead Programmer for complex or multiple studies. Ensure quality, compliance, and efficient execution of programming activities. Make data-driven decisions and proactively address risks and issues. Basic Qualification Bachelor’s degree in Statistics, Computer Science, or a related field. Expertise in R programming. 6+ years of

clinical programing 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. Preferred Qualification Strong experience supporting HIV clinical trials and drug development within the pharmaceutical or biotechnology industry. Advanced degree in Statistics, Computer Science, Data Science, or a related discipline. Experience using generative AI tools and coding assistants (e.g., GitHub Copilot, Claude, or Codex) to improve programming productivity and automation. Familiarity with modern software engineering practices, including Git-based workflows, reusable frameworks, and automation pipelines. Experience with R, Python, and open-source analytics tools within regulated clinical development environments. Experience contributing to standards development, process

improvement, or digital transformation initiatives, Knowledge of Agile delivery methodologies and collaborative product development approaches. Demonstrated experience leading programming activities for complex clinical studies or multiple projects. Strong understanding of CDISC standards, regulatory expectations, and quality/compliance requirements. Excellent analytical, problem-solving, communication, and stakeholder management skills. Experience mentoring or guiding junior team members At ViiV Healthcare, our mission is to ensure that the impact of HIV is minimized for individuals and communities worldwide. We are deeply committed to: Patient Focus - Always putting the needs of those living with HIV first. Transparency, Respect, and Integrity - Maintaining open communication, mutual respect, and a high ethical standard in everything we do. Courage and Accountability - Demonstrating bold leadership by making agile, evidence-based decisions and taking responsibility for outcomes. Development and Teamwork - Investing in our team members’ growth and building collaborative, impact-driven partnerships internally and externally. As part of our 30-year legacy of improving lives with HIV, ViiV Healthcare is not just a place to work-it is a community where every team member is empowered to bring their very best to the fight against HIV/AIDS. Our holistic approach extends beyond medicine to supporting sustainable community programs and improving access to care. #J-18808-Ljbffr