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This position was posted on May 21, 2026 and is likely no longer accepting applications. We've kept it here for historical reference. Check out the similar jobs below!
Job Overview
Location
Your Remote US Home Office
Job Type
Full-time
Category
Data & Analytics
Date Posted
May 21, 2026
Full Job Description
đź“‹ Description
- • The Senior Statistical Programmer Analyst prepares analysis programs to support the preparation and statistical analysis of clinical data, coordinates statistical programming activities for multiple clinical projects, ensures internal consistency of output, and assesses consistency with other projects and activities.
- • Day-to-day responsibilities include developing algorithms and writing programs to create datasets, producing data listings, summary tables, and graphs using analysis software, independently checking outputs, importing and exporting data, assisting data management with data edit checks, maintaining expertise in CDISC and FDA guidance, preparing clinical trial datasets for regulatory submission, writing specifications for analysis datasets, interacting with project statisticians and other programmers, managing the clinical data warehouse, interacting with regulatory affairs and quality assurance staff, mentoring less experienced programmers, acting as a subject matter expert on CDISC and good statistical programming practices, building efficient SAS coding and macro libraries, ensuring work adheres to GCP, ICH, 21 CFR part 11, internal SOPs, and international regulatory requirements, adhering to the Company’s Quality Management System, and ensuring departmental compliance with QMS and regulations.
- • Penumbrainc Inc. is a company focused on clinical data analysis and regulatory submission, operating in the medical device, biotechnology, pharmaceutical, or CRO industries, with a commitment to quality, compliance, and innovation in clinical data standards.
- • The role offers the opportunity to deepen expertise in clinical data standards (CDISC, SDTM, ADaM, etc.), lead statistical programming efforts across multiple projects, mentor junior staff, influence regulatory submission quality, and become a recognized subject matter expert in SAS-based clinical data programming and compliance within a regulated industry environment.
🏖️ Benefits
- • Annual Base Salary Range: $140,000 - $191,000
- • Competitive compensation package plus benefits and equity program, when applicable
- • Remote work opportunity (Your Remote US Home Office)
- • Opportunity to mentor less experienced statistical programmers and act as a subject matter expert
- • Engagement with regulatory affairs, quality assurance, and external clinical system vendors
- • Work aligned with GCP, ICH, 21 CFR part 11, and international regulatory requirements
Skills & Technologies
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About Penumbrainc Inc.
Penumbrainc is a biotherapeutics company advancing precision-engineered antibodies that modulate the complement system to treat severe autoimmune and inflammatory diseases. Its lead programs target dysregulated complement activation underlying conditions such as paroxysmal nocturnal hemoglobinuria, cold agglutinin disease, and Guillain-Barré syndrome. The company applies structural biology insights to create long-acting, subcutaneous therapies with improved safety and dosing convenience over existing intravenous treatments. Founded in 2020 and headquartered in South San Francisco, Penumbrainc is advancing candidates through preclinical and early clinical development with the goal of delivering first-in-class complement inhibitors to patients with high unmet medical need.
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