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About the Role

The Statistical Programmer supports programming activities for multiple projects on clinical study reports and publications. This role is accountable for clinical statistical programming deliverables, ensuring excellence in quality and timelines for clinical trials under Statistics & Data Management. The programmer will collaborate with various teams to clarify requirements and resolve data or programming issues, contributing to the development of best-in-class programming outputs for new products and therapies.

Responsibilities

Support programming activities for multiple projects on clinical study reports and publications
Accountable for clinical statistical programming deliverables, ensuring excellence in programming activities in terms of quality and timelines for clinical trials
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
Produce 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

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
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 SAS Enterprise Guide or other SAS-based clinical programming environments (Desired)
Experience supporting medical device, neuromodulation, or cardiovascular/respiratory studies (Desired)
Familiarity with data visualization, dashboards, automation, or workflow improvement (Desired)
Experience working with vendors or cross-functional global teams (Desired)
Understanding of controlled programming environments, SOPs, and audit-ready documentation (Desired)

Skills

SAS programming (data step, procedures, macros, debugging)
R
Python
SQL
Git

Work Type

Flexible Work Schedules

Experience Level

Relevant experience in clinical trial programming, clinical data analysis, statistical programming, or regulated data environments

Education Level

Bachelor’s degree or higher in statistics, mathematics, computer science, life sciences, data science, or related field

Salary/Compensations

$90,000 - $100,000 annual base salary plus discretionary annual bonus

Benefits

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

About the Company

Global medtech company driven by a vision to change the trajectory of lives and a mission to create ingenious solutions that ignite patient turnarounds.
Committed to patients and innovation in healthcare.
A people-oriented company with employees committed to improving quality of life for patients and their families.