Statistical Programmer II

The Role

• The Statistical Programmer will support programming activities for multiple projects on clinical study reports and publications.
• Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of Statistics & Data Management.
• Collaborate with Statistics, Data Management, Clinical, and vendor teams to clarify requirements and resolve data or programming issues.
• Develop, validate, and maintain SAS programs in accordance with study requirements, internal standards, and SOPs.
• Contribute to the creation, validation, and documentation of SDTM and ADaM datasets.
• Responsible for producing programming outputs, validation, and related documentation to ensure accuracy, consistency, and traceability.
• Ensure deliverables meet expectations in terms of timelines and quality, regulatory and key user group requirements (e.g., CDISC), operational efficiency, and alignment with the study's clinical and statistical objectives.
• Provide input into SAP, analysis specifications, and data presentations for clinical trials.
• Support ongoing workflow modernization, migration activities, and standardization initiatives.
• Participate in process improvement activities related to programming efficiency, quality, and standardization.

• Bachelor’s degree or higher in statistics, mathematics, computer science, life sciences, data science, or related field.
• Relevant experience in clinical trial programming, clinical data analysis, statistical programming, or regulated data environments.
• Strong SAS programming skills, including data step, procedures, macros, and debugging.
• Ability to write clear, validated, reusable, and well-documented code.
• Understanding of programming quality control, validation, and traceability expectations.
• Working knowledge of CDISC standards, especially SDTM and ADaM.
• Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses.
• Understanding of clinical trial data flow from data collection to analysis/reporting.
• Strong attention to detail and quality.
• Ability to work independently on assigned tasks with appropriate guidance.
• Good communication skills and ability to collaborate with Statistics, Data Management, Clinical, and external vendors.
• Ability to manage priorities and timelines in a changing project environment.

• Experience with R, Python, SQL, Git, or other modern programming/version control tools.
• Experience with SAS Enterprise Guide or other SAS-based clinical programming environments.
• Experience supporting medical device, neuromodulation, or cardiovascular/respiratory studies.
• Familiarity with data visualization, dashboards, automation, or workflow improvement.
• Experience working with vendors or cross-functional global teams.
• Understanding of controlled programming environments, SOPs, and audit-ready documentation.

• A reasonable estimate of the annual base salary for this position is $90,000 - $100,000 plus discretionary annual bonus. Pay ranges may vary by location and are awarded based on experience.

• Health benefits – Medical, Dental, Vision
• Personal and Vacation Time
• Retirement & Savings Plan (401K)
• Employee Stock Purchase Plan
• Training & Education Assistance
• Bonus Referral Program
• Service Awards
• Employee Recognition Program
• Flexible Work Schedules