Sr Director, Biostatistics - Oncology Programs

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

Position Overview:

Reporting to the Head of Oncology Biostatistics, the Senior Director of Biostatistics will lead, manage, and develop a team of statisticians supporting late‑stage oncology development. This role provides strategic statistical leadership and oversight across development planning, regulatory interactions, and HTA/commercial evaluations for one or more Gilead oncology assets/indications. The ideal candidate brings a strong track record of functional leadership, deep expertise in statistical methods for drug development, and demonstrated excellence in people leadership and talent development.

Job Responsibilities and Skills:

• Provide strategic statistical leadership for late-stage (Phase 3) oncology clinical trials, including design optimization and high-quality quantitative decision support.
• Serve as the Biostatistics statistical lead for assigned oncology molecules/indications, representing the function in Health Authority interactions and ensuring clear accountability and alignment with the Therapeutic Area Head.
• Partner cross-functionally with Statistical Programming, Clinical Research, Data Management, Clinical Operations, Global Drug Safety, Regulatory, and Project Management to deliver high-quality analyses and clinical reports on time and to standard.
• Apply statistical and regulatory principles to achieve scientific, regulatory, and business objectives; contribute to regulatory strategy and risk assessment; and support publications and external scientific presentations while proactively managing timelines and resources.
• Lead, mentor, and develop high-performing teams of experienced statisticians, including ownership of staffing strategy, succession planning, and long-term workforce planning.
• Leverage competitive intelligence and strong external scientific/regulatory networks (academia, industry, and Health Authorities) to inform development strategy, elevate scientific credibility, and enhance organizational visibility.
• Demonstrate strong judgment, decision-making, communication, and influencing skills, with the ability to drive alignment and execution across functions in complex, fast-paced, and ambiguous environments.
• Build effective partnerships within Biostatistics and across cross-functional stakeholders, fostering collaboration, shared accountability, and a culture of excellence.

Basic Qualifications:

Preferred Qualifications:

• PhD with 12+ years or MS with 14+ years of biostatistics or statistical analysis experience in the pharmaceutical or biotechnology industry, including at least 5 years in oncology drug development.
• Strong hands‑on experience in oncology clinical development, including design and analysis of late‑stage (Phase 3) trials and leadership of NDA and/or BLA submissions.
• Demonstrated extensive experience interacting with global Health Authorities and contributing to regulatory strategy and labeling discussions.
• Deep expertise in biostatistics, with proficiency in industry‑standard statistical software and application of current methodologies to improve study design, data quality, and decision making.
• Proven people‑management experience, including leading, mentoring, and developing teams of experienced statisticians.
• Solid understanding of the broader biopharmaceutical business, with recognized scientific or strategic credibility beyond Biostatistics.

 

The salary range for this position is: $261,375.00 - $338,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

For jobs in the United States:

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