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Statistical programmer • durham nc

Última actualización: hace 4 días

Principal Statistical Programmer

10480 vii v healthcare Durham Blackwell Street
A tiempo completo

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 • Oferta promocionada

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Principal Statistical Programmer

Principal Statistical Programmer

10480 vii v healthcareDurham Blackwell Street
Hace más de 30 días
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

ViiV Healthcare is a global specialty HIV company wholly committed to researching and delivering new medicines for people living with–and at risk of–HIV. As the Senior Medical Director, you will play a pivotal role in advancing our mission to leave no patient behind by ensuring clinical excellence in early development programs (with a focus on long-acting medicines) and providing medical governance for Phase 1–4 studies. You will work in a fast-paced, diverse, inclusive, and high-performing team that is dedicated to delivering breakthroughs in HIV care.


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.


This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

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.
  • Contribute to departmental initiatives and technical strategy.

Quality & Compliance

  • Ensure adherence to standards (e.g., GPP, CDISC) and regulatory requirements.
  • Perform QC on critical outputs and technical documents (e.g., cSDRG, ADRG).
  • Maintain governance and oversee TMF compliance.

Strategy & Innovation

  • 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.

Communication & Mentorship

  • Communicate technical concepts, risks, and timelines clearly to stakeholders.
  • Mentor junior programmers and share best practices internally and externally.

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.

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.

Why You:

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.

#LI-ViiV