Non-Clinical Jobs: Sanofi is Hiring a Principal Non-Clinical Biostatistician | Apply Now for Sanofi career | Pharma Jobs
Are you looking for pharma jobs? Step into a career where science meets innovation with Sanofi career. Hiring a Principal Non-Clinical Biostatistician at the Hyderabad hub. This non-clinical job role offers the opportunity to lead statistical strategies across non-clinical studies, collaborate with top scientific minds, and impact millions worldwide through meaningful data-driven insights.
Job Details:
- Job Title: Principal Non-Clinical Biostatistician
- Location: Hyderabad, India
About Sanofi:
Sanofi is a global healthcare leader dedicated to chasing the miracles of science to improve people’s lives. Headquartered in Paris, Sanofi operates in over 100 countries, pioneering breakthroughs in biopharmaceuticals, vaccines, rare diseases, oncology, immunology, and neurology. The company integrates cutting-edge research, data science, and AI-driven discovery to bring innovative therapies to patients worldwide.
With a strong focus on diversity, sustainability, and continuous innovation, Sanofi empowers its people to pursue progress and make a meaningful impact in global healthcare.
Education:
- Master’s or Ph.D. in Pharmaceutical or related field with relevant industry experience.
- Proven expertise in non-clinical statistics applied to biopharmaceutical development.
- Strong knowledge of industrial statistics, design of experiments, multivariate analysis (PCA, PLS), and modeling.
Key Responsibilities:
- Lead statistical analysis for non-clinical studies, ensuring data quality and compliance with Sanofi standards.
- Perform data analyses using R, SAS, JMP, SIMCA, and other statistical tools to generate reports and insights.
- Review study designs, reports, and study plans, ensuring alignment with best practices.
- Develop and support end-user tools like RShiny to enhance data interpretation.
- Contribute to the development of advanced statistical methodologies and innovative approaches.
- Determine optimal design and sample size for in vivo experiments under Animal Welfare Committee (AWC) guidelines.
- Present statistical findings to cross-functional teams and senior leadership.
- Ensure adherence to internal standards, external guidelines, and global regulatory requirements.
Technical Skills:
- Proficient in R, SAS, JMP, SIMCA, MODDE.
- Experience with CMC regulatory guidelines (EMA, FDA, ICH Quality).
- Knowledge of QbD principles and preparation of statistical analysis for regulatory dossiers.
Soft Skills:
- Excellent interpersonal and communication skills.
- Ability to work in cross-functional and global teams.
- Strong analytical mindset with attention to detail and innovation.
Languages:
Proficient in English (oral and written).
