Senior Statistical Programmer

Johnson & Johnson

Confirmed live yesterday High trust

Remote

Quick summary

Work type: Remote
Location: Santa Clara, CA
Salary: $92,000–$148,350 / yr
Employment: Full-time
Posted: 14 days ago
Freshness: Confirmed live yesterday
Nearby: 99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $184k

This role $120k

$76k $241k

below market most similar roles pay here above market

This role pays less than 97% of similar roles. Most pay $158,025–$209,133 — the blue band above. At the midpoint, this role pays about $120k versus about $184k for comparable roles.

Based on 240 similar postings.

Employer

About Johnson & Johnson

Johnson & Johnson is a multinational corporation operating in three main segments: consumer health products, pharmaceuticals, and medical devices, known for brands like Tylenol, Band-Aid, and Janssen. Industry: Pharmaceuticals & Medical Devices

Johnson & Johnson currently has 46 open roles on FindRole.

Listed pay typically runs $113,000–$201,250 across 38 roles with salary data.

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At a glance

TL;DR · Senior Statistical Programmer

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The Senior Statistical Programmer joins the Biostatistics team to support the MedTech Circulatory Restoration Portfolio. This role involves generating and validating analysis datasets and statistical outputs for clinical trials, specifically supporting the development of Intravascular Lithotripsy to treat calcified cardiovascular disease. Key responsibilities include developing SAS programs to produce tables, listings, and figures for regulatory submissions, maintaining standardized programming templates, and ensuring CDISC-compliant datasets like SDTM and ADaM. The candidate will perform quality control, document programming activities for audit readiness, and collaborate with cross-functional teams on data cleaning and interim analyses. Required technical skills include proficiency in SAS programming (Base, Macro, SQL), exposure to SAS Graph and Stat procedures, and knowledge of GxP principles and FDA/EMA regulatory requirements for medical device submissions such as PMA and 510(k).

Skills

SAS SQL R CDISC SDTM ADaM Biostatistics Data Analytics Statistical Programming Data Visualization Version Control GxP Clinical Trial Design Data Modeling PMA 510(k)

What you'll do

Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures for clinical trial reporting.
Implement and maintain standardized programming templates, macros, and tools to ensure consistency and compliance across studies.
Create and review programming specifications for SDTM and ADaM datasets based on CDISC standards.
Perform quality control and validation of internally and externally developed datasets and outputs according to company SOPs.
Integrate data across multiple studies for pooled analyses and visual summaries to support regulatory filings.
Document all programming activities clearly to support reproducibility and regulatory compliance in a validated environment.
Create visual data summaries and contribute to posters or presentations using SAS graphics and other visualization tools.

What we're looking for

Bachelor’s degree or higher in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline.
5+ years of experience in statistical programming within the pharmaceutical, biotechnology, or medical device industry.
Proficiency in SAS programming (Base, Macro, SQL) with exposure to SAS Graph and Stat procedures.
Experience with R or data visualization (preferred).
Understanding of clinical trial design, GxP principles, and FDA/EMA regulatory requirements for medical device submissions.
Familiarity with CDISC standards (SDTM, ADaM) and ability to implement standardized datasets.
Strong attention to detail, problem-solving mindset, and effective communication skills.
Experience with advanced analytics, biological sciences, and data modeling (preferred).

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