Principal Statistical Programmer
Location
Andhra Pradesh | India
Job description
About the role
Principal Statistical Programmer
Location: Hyderabad, India #LI-Hybrid
About the Role:
The Statistical Programming team is a dynamic function where we are empowered to experiment, explore and progress beyond the boundaries of best-in-class Statistical Programming analysis. From a collaborative effort with Data Management, Clinical Study Teams, Statisticians, medical / scientific writing teams, publication teams, we analyze tons of data, deriving meaningful insights that enable us to deliver innovative medicines to millions of patients worldwide.
Your key responsibilities:
Your responsibilities include, but are not limited to:
• Responsible for managing project level activities within Product Lifecycle Services (PLS). Act as the programming functional lead on customers' project teams. Participate in project team meetings. Determine an efficient project programming strategy that utilizes customers' standards and procedures. Develop project-level programming specifications for analysis datasets and pooled datasets for a project.
• Lead the production of statistical outputs for clinical study reports, publications, and market promotions. Ensure the quality control of all programs, specifications and statistical outputs within a study project.
• Ensure that programming-related documents are consistent, and comply with Data Science's and customers' standards, by reviewing case report forms, statistical analysis plans, data structures specifications, and specifications for tables, listings and figures. Archival of project programs and associated documentation.
• Mentor programmers in the functional expertise required for project support. Support the development of, and the training of users in, new programming applications.
• Develop advanced, general-purpose programming functions for deployment across multiple projects. Maintain advanced knowledge of programming languages (e.g., SAS and R).
• Manage the outsourcing of programming activities from Data Science to an approved vendor in accordance with Scientific Services vendor management procedures.
Role Requirements
Essential:
• Proven experience in development of advanced programming functions with high programming efficiency; strong programming and problem-solving skills
• Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent) .
Desirable requirements:
• Good understanding of global clinical trial / project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. Good Clinical Practice).
• Good knowledge of office tools.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:
You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.
Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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