Statistical Programmer Jobs in New York (NOW HIRING)

The Position The purpose of this role is to lead and contribute to statistical programming activities across SDTM, ADaM, and Tables, Listings, and Figures (TLFs), providing both technical oversight and hands-on support for the development, validation, and programmatic review of datasets and outputs. This role ensures the quality, consistency, and timeliness of deliverables supporting oncology regulatory submissions by guiding programming strategies, reviewing key outputs, and driving issue resolution. In addition, this position fosters and maintains institutional knowledge across oncology compounds, while supporting the development, standardization, and continuous improvement of programming processes and best practices for datasets and TLFs to enhance efficiency, quality, and compliance.

Roles and Responsibilities Lead and Execute Statistical Programming Develop and validate datasets and Tables, Listings, and Figures (TLFs) to ensure high-quality deliverables for pivotal studies, as well as Integrated Summary of Efficacy (ISE) and Integrated Summary of Safety (ISS) for oncology regulatory submissions Drive end-to-end programming from SDTM through ADaM to TLF generation in compliance with CDISC standards and regulatory requirements Develop SDTM CRF annotations and SDTM specifications, as well as analysis dataset specifications to ensure accurate implementation of SAPs and TLF shells Perform hands-on programming to create and validate SDTM and ADaM datasets and TLFs, ensuring quality, integrity, and submission readiness Ensure datasets meet CDISC and regulatory submission standards while conducting comprehensive reviews of submission data packages to ensure quality, completeness, and alignment with regulatory expectations Manage and Coordinate Statistical Programming Activities Develop and manage programming timelines and resource plans Collaborate closely with Biostatistics, Data Management, and cross-functional teams to ensure efficient and accurate execution Manage the generation and tracking of datasets and TLFs for ongoing and completed studies, ensuring appropriate data usage and high-quality outputs Proactively identify and resolve programming-related issues prior to database lock and analysis Ensure the completeness and accuracy of all study programming deliverables Maintain all required programming documentation in compliance with Trial Master File (TMF) requirements Oversee Statistical Programming Vendor (Outsourced Studies) Review and agree on vendor project timelines and resource planning Work in tandem with Biostatistics and Data Management members to ensure best vendor performance Monitor analysis dataset and TLF transfers for ongoing and completed trials, confirming data use and output quality Proactively ensure the resolution of programming-related issues prior to database lock and analysis Verify completeness of study programming deliverables and maintain all required study programming documentation for the Trial Master File (TMF) Maintain Institutional Knowledge and Standardized Programming Practices: Contribute to CRF and SDTM standard development Support the development, implementation, and maintenance of Analysis Data Model (ADaM) datasets and TLF standards Support training initiatives to ensure consistent implementation of ADaM and TLF standards in clinical trial analyses Provide Programming Support for Regulatory Activities Develop TLFs to support submission-related queries with quick turnaround timelines Support ad hoc and exploratory analyses requested by clinical teams Provide programming support for regulatory responses and potential Advisory Committee meetings Develop and Maintain Programming Macros Collaborate with Biostatistics team members to define requirements for efficacy data review Develop and enhance macros Support internal data review and monitoring activities Qualifications Education Qualifications Master's Degree Biostatistics or similar degree required PhD Biostatistics or similar degree preferred Experience Qualifications 6+ years of proven experience within pharmaceutical industry, or CROs supporting statistical analysis of clinical trials programming with a master’s degree required Oncology experience required Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming preferred Advanced working knowledge of CDISC SDTM and ADaM, and extensive experiences of their implementation in clinical trials analysis preferred Advanced understanding of statistical concepts in support of analyses and reporting of clinical trials preferred Knowledge of all phases of drug development, including early and late phase clinical development and global submission preferred Experience with R and Python programming languages preferred Familiarity with AI/ML and their applications in clinical data analysis preferred Experience supporting and maintaining Statistical computing environment and clinical data repository system preferred Travel Requirements Ability to travel up to 10% of the time Why work with us? Working at Daiichi Sankyo is more than just a job – it is your chance to make a difference and change patients’ lives for the better. We can only achieve this ambitious goal together.

That is why we foster a culture of mutual respect and continuous learning, with a strong commitment to inclusion and diversity. Here, you will have the opportunity to grow, think boldly, and contribute your ideas. If you have a proactive mindset and passion for addressing the needs of patients, we eagerly await your application.