Job Information
Sanofi Group Senior Statistical Programmer - R&D in India
Job title: Senior Statistical Programmer - R&D
Location : IN / Hyderabad
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 Senior Statistical Programmer, you’ll plan and execute high quality and timely statistical programming deliverables within a study in the early development portfolio.
Study Statistical Programmer (SP) of a study, with direction from study lead programmer or programming project leader, execute statistical programming activities for the responsible study.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities :
Perform programming activities for all statistical deliverables within a study, e.g. SDTM, ADaM, Tables Listings and Figures (TLF) for Data Monitoring Committee Reports (DMC, if any), Interim Analysis (if any), Clinical Study Report, Transparency (Eudract, CTGov, Lay Summary), Statistical Surveillance, Publications and any exploratory analyses.
Perform quality control for statistical programming deliverables and completes the associated documentation: Validation plan and quality control (QC) documentation.
Review and provide feedbacks on study documents, such as protocol (statistical section), Case Report Form (CRF), Statistical Analysis Plan (SAP) and Table Listing and Figures (TLF) templates.
Write and provide the programming specifications for the Study Data Tabulation Model (SDTM) and Analysis Datasets Model (ADaM) for a study.
Ensure compliance to SOP’s, standards, and guidelines.
Collaborate with study team members
About you
Experience : Experience in programming experience preferably in processing clinical trial data in the pharmaceutical industry
Knowledge about early phase clinical development programs
Soft Skills & Technical Skills : Technical skills in statistical programming, with at least intermediate proficiency in R (and SAS), in a clinical data environment
Excellent knowledge of Good Programming Practices
Ability to perform the preparation, execution, reporting and documentation of all programming deliverables of a study.
Ability to work in team environment.
Ability and mindset to embrace change, innovate and continuously improve programming practice.
Education : Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field.
Language : Good written and verbal communication skills in an English global environment
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Join an international biopharma company
Act within an international team on safety analytic domain, to deliver solutions for data integration and data visualization.
Work on several compounds for multiple clinical therapeutic areas
Join the Early Development Hyderabad Capacity Center as a Senior Statistical Programmer and play a pivotal role in executing high-quality deliverables that drive innovation and contribute global health improvements, all while advancing your career in a supportive, growth-oriented environment. ”