Associate Biostatistics Director

Gilead Sciences, Inc.; Foster City (CA); On-site; USD 90,000 - 160,000; Full time

Job summary

An established industry player is seeking an Associate Biostatistics Director to lead biostatistical analysis and reporting for clinical studies. This role involves collaborating with cross-functional teams to ensure timely NDA submissions, providing statistical consultation on trial design, and contributing to the development of biostatistical strategies. The ideal candidate will have a PhD in biostatistics or a related field, with significant experience in statistical analysis using SAS software. Join this innovative firm and help shape the future of healthcare by transforming data into actionable insights.

Qualifications

• PhD in biostatistics or related field with relevant experience in statistical analysis.
• Experience in managing cross-functional projects in biopharma.

Responsibilities

• Lead biostatistical analysis and reporting for NDA submissions.
• Collaborate with cross-functional partners to meet project timelines.

Skills

Statistical Analysis

Project Management

SAS Software

Biomedical Statistical Analysis

Communication Skills

Strategic Thinking

Education

PhD in Biostatistics

MS in Biostatistics

Tools

Statistical Software

Data Management Tools

Job description

Associate Biostatistics Director

United States - California - Foster City Clinical Development & Clinical Operations Regular

Job Description

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

The Associate Director, Biostatistics will lead biostatistical analysis and reporting, document review and data inclusion for NDA submissions of assigned studies by collaborating with cross-functional partners to meet clinical development project deliverables and timelines. This may include, but is not limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical study endpoints, calculating sample size, authoring statistical analysis plans and providing biostatistical input into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, the position may lead projects or other activities that are non-molecule based, such as Biostatistics tools, programming, centralized analyses and reporting, etc. The Associate Director will also contribute to short- and long-range Biostatistics strategies, plans and infrastructure development that transcend multiple areas and teams across Biostatistics, such as team capability development.

Responsibilities:

• Acts as biostatistics lead on clinical studies or other non-molecule projects.
• Where applicable, leads statistical analysis, document review and data inclusion for NDA submissions of assigned studies by collaborating with other Biostatistics team members and cross-functional partners. Provides statistical consultation on trial design and study endpoints and authors statistical analysis plans.
• Where applicable, oversees and contributes to completion of all technical and operational statistical activities for a group of clinical trials.
• Where applicable, participates in cross-functional clinical development planning for one or more molecules or marketed products to provide the biostatistical perspective and biostatistical input.
• Where applicable, participates in cross-functional protocol design and review discussions.
• Where applicable, advises internal and external partners as to choice of statistical analysis strategies, reliability of measurements and identifiability of models, and interpretation and presentation of statistical results.
• Leads the gathering, organization and analysis of different data sources to enable delivery of special projects and/or the statistical analysis plan and clinical study endpoints for assigned products.
• Reviews and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring.
• Uses a variety of advanced statistical software, methods, and techniques to gather, analyze, and interpret research data to derive useful information for clinical development.
• Plans and documents computer data file structure; develops, programs, manages, and maintains complex statistical databases; performs or supervises data entry.
• Develops enhancements to statistical software, as appropriate, by programming new techniques; maintains knowledge of current and emerging trends in statistical analysis methodologies and tools.
• Provides biostatistical input into clinical development documentation, scientific publications and presentations and regulatory documentation.
• May participate in or lead special projects that can benefit multiple Biostatistics team members.
• Independently defines required resources for assigned work, seeking advice as needed.
• Adheres to regulatory requirements of study conduct, statistical analysis principles, industry standards, and Gilead SOPs.

REQUIREMENTS:

PhD in biostatistics or related discipline with 2+ years’ relevant experience in statistical analysis of biomedical data using SAS software in the biopharma industry or a related environment. PhD with 4+ years’ biostatistics experience is preferred.

MS in biostatistics or related discipline with 8+ years’ relevant experience in statistical analysis of biomedical data using SAS software.

Minimum of 2 years’ cross-functional project management or leadership experience in biostatistics or a related field in the biopharma industry or a related environment, including multiple years’ experience managing project teams.

Significant biomedical statistical analysis experience and experience working with relevant software.

Experience developing software and other tools to support statistical analysis of biomedical or related data. Strong proficiencies in software and other tools used typically used by Biostatistics.

Proven effectiveness managing projects and teams.

Knowledge & Other Requirements

• Demonstrated ability to be a fast learner.
• Demonstrated ability to be flexible and adaptable to change.
• Has advanced knowledge of biomedical statistical analysis.
• Has advanced knowledge of biostatistics best practices and tools.
• Demonstrates strategic thinking in advising others on statistical requirements and opportunities to improve study or other project outcomes.
• Understands drug development phases and the nature of associated clinical trials across phases.
• Knowledge of FDA and EMA regulations, ICH guidelines, GCP and familiarity with standard clinical procedures.
• Strong communication and organizational skills.
• When needed, ability to travel.