Senior Principal Statistical Programmer

As a Statistical Programming Lead at the company, your key responsibilities will include: - Leading statistical programming activities for multiple studies and driving the implementation of data analytics reports. - Making decisions and proposing strategies at the study or project level. - Acting as a functional manager for local associates, providing supervision and advice on functional expertise and processes. - Building and maintaining effective working relationships with cross-functional teams, summarizing and discussing the status of deliverables and critical aspects. - Ensuring project-level standardization, providing and implementing programming solutions, and ensuring knowledge sharing. - Acting as an expert in problem-solving aspects. - Ensuring timely and quality development and validation of datasets and outputs for regulatory submissions/interactions, safety reports, publications, post-marketing activities. - Leading or co-leading novel projects within the team. - Generating creative ideas within your team and/or project team/functional community. - Recognizing and leveraging innovation opportunities for your team across projects. - Mentoring and inspiring others to solve problems. - Reporting technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt. - Distributing marketing samples where applicable. Your performance will be measured based on: - Achieving a high level of quality, timeliness, cost efficiency, and customer satisfaction across functional activities and deliverables. - Adherence to Novartis policy and guidelines. - Customer/partner feedback and satisfaction. Minimum Requirements: - Work Experience in Biostatistics, Clinical Research Phases, R&D Portfolio Management, Statistical Programming, Data Management & Systems, Regulatory Submissions, Creative & Analytical Technologies, and Clinical Trial Design, Data Review & Reporting. Skills required for this role include proficiency in Classification Systems, Clinical Trials, Computer Data Storage, Computer Programming, Cross-Functional Teams, Data Analysis, Data Structures, Initiative, Programming Languages, Reporting, and Statistical Analysis. As a Statistical Programming Lead at the company, your key responsibilities will include: - Leading statistical programming activities for multiple studies and driving the implementation of data analytics reports. - Making decisions and proposing strategies at the study or project level. - Acting as a functional manager for local associates, providing supervision and advice on functional expertise and processes. - Building and maintaining effective working relationships with cross-functional teams, summarizing and discussing the status of deliverables and critical aspects. - Ensuring project-level standardization, providing and implementing programming solutions, and ensuring knowledge sharing. - Acting as an expert in problem-solving aspects. - Ensuring timely and quality development and validation of datasets and outputs for regulatory submissions/interactions, safety reports, publications, post-marketing activities. - Leading or co-leading novel projects within the team. - Generating creative ideas within your team and/or project team/functional community. - Recognizing and leveraging innovation opportunities for your team across projects. - Mentoring and inspiring others to solve problems. - Reporting technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt. - Distributing marketing samples where applicable. Your performance will be measured based on: - Achieving a high level of quality, timeliness, cost efficiency, and customer satisfaction across functional activities and deliverables. - Adherence to Novartis policy and guidelines. - Customer/partner feedback and satisfaction. Minimum Requirements: - Work Experience in Biostatistics, Clinical Research Phases, R&D Portfolio Management, Statistical Programming, Data Management & Systems, Regulatory Submissions, Creative & Analytical Technologies, and Clinical Trial Design, Data Review & Reporting. Skills required for this role include proficiency in Classification Systems, Clinical Trials, Computer Data Storage, Computer Programming, Cross-Functional Teams, Data Analysis, Data Structures, Initiative, Programming Languages, Reporting, and Statistical Analysis.