Senior Statistician I

Senior Statistician I

Choosing Capgemini means choosing a place where you’ll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what’s possible. Join us in helping leading healthcare and life sciences organizations unlock the value of data and drive evidence-based, impactful research.

Your Role

We are seeking an experienced and collaborative Senior Statistician I to provide advanced statistical expertise and leadership in support of clinical research studies. This role involves working closely with Biostatisticians, Statistical Programmers, Clinical Data Managers, and sponsor teams to ensure the accuracy, reliability, and regulatory compliance of statistical deliverables. The Senior Statistician will also oversee quality control processes and contribute to the development of statistical analysis plans and datasets.

In this role, you will:

• Provide statistical leadership and support for clinical trials, ensuring high-quality deliverables.
• Participate in cross-functional study-related activities and team meetings.
• Perform sample size calculations and author or review statistical analysis plans (SAPs).
• Coordinate with Biostatisticians, Statistical Programmers, and Data Managers to prepare, conduct, and review statistical analyses.
• Ensure the accuracy and integrity of final statistical outputs and deliverables.
• Guide and supervise programmers in developing analysis specifications and programming/validation of tables, listings, figures (TLFs)/ CDISC Standards/SDTM/ADAMs
• Validate analysis variables/statistical outputs for consistency/compliance.
• Conduct quality control (QC) of data displays/analysis datasets prepared by others.
• Maintain project administration files including protocols, annotated CRFs, SAPs, annotated shells, programming/QC rules, tracking logs, communications.
• Participate in internal meetings/contribute to Biostatistics Development Team initiatives.
• Statistical Methodology: Advanced statistical techniques, sample size estimation, inferential statistics
• Programming: Proficiency in SAS, Macros Base SAS, clinical data analysis tools

Your Profile

• Master’s degree in Statistics or related field with 6+ years of industry experience
• PhD in Biostatistics or related field with 3+ years of postgraduate experience
• Proven ability to lead projects and manage cross-functional teams
• Strong foundation in statistical methodologies and SAS programming
• Experience with clinical trial data analysis and regulatory submissions

What You’ll Love About Working Here

We value flexibility and support our employees with Hybrid work options and adaptable schedules to maintain a healthy work-life balance. Our inclusive culture brings together diverse professionals committed to growth, innovation, and excellence. You’ll have access to continuous learning opportunities and certifications in emerging technologies and methodologies.

About Capgemini

Capgemini is a global business and technology transformation partner, helping organizations accelerate their dual transformation to address the evolving needs of customers and citizens. With a strong 55-year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needs—from strategy and design to operations.To achieve this, Capgemini draws on the capabilities of its 360,000 team members in more than 50 countries, all driven by the purpose of unleashing human energy through technology for an inclusive and sustainable future. It is a responsible and diverse organization with market-leading capabilities in digital, cloud, and data.