Senior Statistical Programmer Analyst

. Prepare analysis programs supporting the preparation and statistical analysis of clinical data .

Posted 10/15/2026full-timeRemote • United StatesSenior💰 $65 - $115 per hourWebsite

Tools & technologies

Google Cloud PlatformOracleSQL

Key responsibilities & impact

Prepare analysis programs supporting the preparation and statistical analysis of clinical data
Develop algorithms and write programs to create datasets following specifications
Produce and independently check data listings, summary tables, and graphs using analysis software
Import and export data
Assist data management with data edit checks and data cleaning
Maintain understanding of CDISC guidance, implementation guides, and FDA electronic-submission guidance and regulations
Keep current with industry trends in data mapping, data management, standards compliance, metadata management, and data warehousing
Prepare clinical trial datasets and programs for regulatory submission
Write analysis-dataset specifications following statistical analysis plans
Interact with project statisticians and other programmers on project teams
Manage the data warehouse used for clinical study data libraries
Collaborate with regulatory affairs, quality assurance staff, and external clinical system vendors
Mentor less experienced statistical programmers
Serve as subject matter expert on CDISC and statistical programming practices
Build SAS coding and macro libraries
Conduct work consistent with GCP, ICH, 21 CFR Part 11, SOPs, training, and regulatory requirements
Adhere to and help ensure departmental compliance with the Quality Management System and applicable regulations
Perform other work-related duties as assigned

What you’ll need

Bachelor's degree in Statistics, Computer Science, or related field with 5+ years of statistical programming experience and 3+ years of clinical statistical programming experience within the medical device or related industry, or equivalent combination of education and experience
Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, and SAS/STAT
Knowledge of international regulations, requirements, and guidance associated with clinical data standards and clinical databases used for regulatory submission
Knowledge of clinical data standards including CDASH, SDTM, ADaM, SHARE, BRIDG, ODM, Define, and controlled terminology
Knowledge of clinical data management systems, such as Oracle InForm and/or RAVE
Expertise using SAS for data import, manipulation, analysis, export, and graph generation
Proficiency developing SAS macros to access, extract, modify, merge, and analyze clinical data
Strong oral, written, and interpersonal communication skills
High degree of accuracy and attention to detail
Proficiency with MS Word, Excel, and other standard office tools
SAS Certified Base and/or Advanced Programmer experience is preferred
Experience with macro programming, SAS/SQL, metadata repositories, and regulatory submissions is a plus
Ability to handle multiple tasks
Approximately 10% travel to conferences and/or other Penumbra affiliated facilities

Comp & perks

Medical, dental, vision, life, AD&D, short-term disability, and long-term disability insurance
401(k) with employer match
Paid parental leave
Eleven paid company holidays per year
Minimum of fifteen days of accrued vacation per year, increasing with tenure
Paid sick time in compliance with applicable law(s)
Collaborative teamwork environment with constant learning
Performance rewards
Opportunity to contribute to therapies for devastating diseases