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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
 

Title: Senior Manager, Biostatistics

Location: United States – NJ

Biostatisticians work collaboratively with internal and external colleagues to ensure appropriate design, statistical analysis and reporting of Gilead clinical data to efficiently achieve regulatory, scientific and business objectives.

The purpose of this role is to enhance trial design, improve trial conduct, and drive more efficient drug development. We use our statistical expertise, coding skills, and clinical trial design experience to creatively solve meaningful problems and build effective solutions to improve the drug development process. This role will be responsible for research and application of novel statistical methodologies, design and development of innovative analytical tools, and consultation and collaboration to successfully deliver on cross-functional initiatives.

Job Responsibilities

• Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers, Data Scientists, Dev Systems, and other Clinical, Global Drug Safety, Regulatory, IT, and Project Management staff to deliver on cross-functional initiatives and projects.
• Research and support the implementation of innovative trial designs by exploring statistical methodologies, understanding industry best practices, sharing knowledge with cross-functional teams, and supporting the design of innovative trials.
• Serve as a statistical expert for risk-based quality management, with a focus on developing centralized statistical monitoring methods, tools, and processes.
• Design, prototype, and build tools to empower study teams including analytical dashboards, trial simulation packages, data visualizations, and automated workflows.
• Provide statistical support and consulting services for trial design and operations, advanced statistical analyses, portfolio analytics, and other requests, as needed.

Education, Experience, & Skills:
 

• Strong background in statistics, programming, and data analysis
• Hands-on trial statistician experience with trial design, conduct, analysis, and reporting
• Deep and broad knowledge of current statistical methods and drug development best practices
• Expert in R and Python including experience with statistical simulations, package and Shiny development, and machine learning or AI-related use cases
• Highly motivated problem solver with a passion for innovation and process improvement 
• Capable of independent research and creatively designing solutions to complex problems
• Excellent verbal and written communication skills and interpersonal skills
• Can present complicated concepts and proposals in a concise and clear manner to stakeholders
• Team player who enjoys collaborating effectively with internal and external cross-functional teams
• 4+ years of industry experience in clinical trials and an PhD degree in Biostatistics or equivalent OR    6+ years of industry experience in clinical trials and an MS degree in Biostatistics or equivalent OR

8+ years of industry experience in clinical trials and a BS degree in Biostatistics or equivalent

  

  

 

The salary range for this position is: $150,535.00 - $194,810.00. 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.

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As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.
 

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For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.