Data Analysis Programmer

The Principal Statistical Programmer will lead programming activities for one or more studies, ensuring high-quality development, validation, and delivery of complex analysis outputs. Drive technical excellence, innovation, and standards adoption while providing strategic insights into study data. Mentor junior programmers and influence programming approaches through strong technical leadership and communication.Technical Leadership & Delivery Lead programming for studies, ensuring efficient development and validation of analysis packages.Select appropriate tools/languages and solve complex technical challenges.Identify and implement improvements, including use of AI/ML.Quality & Compliance Ensure adherence to standards (e.g., GPP, CDISC) and regulatory requirements.Perform QC on critical outputs and technical documents (e.g., Strategy & Innovation Drive adoption of modern technologies, standards, and Agile practices.Provide technical input on programming strategies and study design.Communication & Mentorship Communicate technical concepts, risks, and timelines clearly to stakeholders.Collaboration & Execution Support sprint planning and project delivery across studies.Collaborate cross-functionally and manage data access appropriately.Support regulatory interactions and contribute to CoE activities.AccountabilitiesServe 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.Why You:Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals:Bachelor's degree in Statistics, Computer Science, or a related field.Expertise in R programming.6+ years of clinical programing experience5+ 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.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.Experience mentoring or guiding junior team membersAt ViiV Healthcare, our mission is to ensure that the impact of HIV is minimized for individuals and communities worldwide. 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.#We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. Born out of a partnership between GSK and Pfizer in 2009, with Shionogi joining in 2012, we are determined to help end the HIV epidemic. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.All employment businesses/agencies are required to contact ViiV's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at SummaryLocation: Durham Blackwell StreetType: Full time