Sanofi Require Senior Biostatistician

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people in over 100 countries at Sanofi are dedicated to making a difference on patients’ daily life, wherever they live and enabling them to enjoy a healthier life.

Post : Senior Biostatistician - Non-Clinical

About the job
Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Non-Clinical Senior Biostatistician within our Statistics Team in Hyderabad, you’ll Support statistical activities for several Non-Clinical efficacy, safety studies or CMC activities, under supervision of statistical team leader.

Main responsibilities
• Contribute to the reliability, scientific quality and optimization of project support from target identification to process development, by providing appropriate Non-Clinical statistical support.
• Accountable for all assigned statistical deliverables related to one or several studies or activities in the Non-Clinical development area.
• Perform statistical analyses of data from the laboratories using R and possibly other languages (SAS, …) or standard statistical software used in Sanofi (JMP, SIMCA, internal tools), to deliver statistical reports/memo
• Review study plans (randomization, sample size, analysis) and reports for internal or external studies (e.g., Statistical Review of SPRs, technical reports, presentations) according to Sanofi best practices
• Contribute to the development and support of statistical end-user tools (mainly RShiny)
• Participate to internal working groups and contribute to develop state-of-the art methodologies and statistical approaches
• Determine optimal design and sample size in particular for in vivo experiments in the scope of Animal Welfare committee (AWC)
• Respect Policies, Standards, external guidelines and processes
• Presentation of statistical work package results to project team members and stakeholders

Candidate Profile
• MS or PhD in Statistics or relevant fields
• (Master) or (PhD) of pharmaceutical or related industry experience
• Languages : Excellent communication in English, both oral and written
• Proven expertise of industrial statistics (descriptive & inferential statistics, statistical process control), design of experiments, multivariate data analysis (PCA, PLS and related methods), statistical modelling and simulation

Soft and technical skills
• Expertise in the field of non-clinical statistics applied to biopharmaceutical development
• Demonstrated excellent interpersonal and communication skills.
• Good knowledge and good understanding of statistical concepts and techniques
• Good knowledge of pharmaceutical research and development
• Able to work in departmental computing environment, can do advanced statistical analyses using SAS, R and other languages.
• Expertise in JMP JSL script; RShiny hosting on GitHub
• Knowledge of CMC regulatory guidelines (EMA, FDA, ICH Quality, Pharmacopeias), QbD principles and ability to prepare statistical analysis for regulatory dossiers.
• Use of standard commercial software e.g. JMP, SIMCA, MODDE

Additional Information
Qualification : MS or PhD
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 10th December 2025