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.

Minimum Requirements

• 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.

Desired Qualifications

• 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.

Pay Transparency

• 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.

Employee benefits include:

• 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