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Sr. Statistical Programmer

Brisbane, CA 94005

Posted: 03/03/2026 Employment Type: Contract Industry: Medical Affairs Job Number: 12541 Pay Rate: $90.00-100.00 Remote Friendly: remote

Job Description

Our client is focused on advancing first- or best-in-class medicines for childhood and adult diseases.

POSITION SUMMARY:

This position is fully remote with a requirement to work on Pacific Standard Time when requested.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Validate and create SDTM, ADaM, and Tables, Figures, and Listings (TFLs), including associated documentation like define.xml using SAS
  • Write or review data specifications for Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM)
  • Hands-on statistical programming to support CSR, publications, presentations, DSUR, IB update, safety data review, reconciliation, ad hoc analyses, patient profiles, and monthly safety reports in a fast-paced environment
  • Ensure that all programming and data are conducted in compliance with GCP, relevant SOPs, and regulatory requirements
  • Assist in the development of template programs or macros and standard specifications to improve efficiency in the Statistical Programming group
  • Work on multiple tasks at same time and prioritizes tasks to meet timelines on a regular basis
  • Collaborates with Biostatisticians, Clinical Data Management, and Clinical Research Scientists on studies when needed
  • Support RWE data curation and summaries in coordination with Biostatistics
  • May assist with testing R and relevant R packages to either validate or develop R-based code solutions

Job Requirements

QUALIFICATIONS:
  • Bachelor’s or higher degree in Statistics, Math or Computer Science or other suitable qualification related to the field
  • 8+ years of statistical programming experience in the pharmaceutical industry
  • Strong SAS programming and statistical background along with experience with Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS
  • Basic level of R knowledge or experience using R and relevant R packages (tidyverse, admiral, etc.) is preferred
  • Thorough understanding of clinical trial design as well as regulatory reporting requirements including electronic data submissions and CDISC implementation
  • Experience working with oncology trials, PK analysis, and NDA or BLA submissions
  • Excellent verbal and written communication skills and interpersonal skills are required
  • Strong hands-on programming skills to deliver results in a fast-moving environment with the ability to work independently when only given loosely defined specifications

Meet Your Recruiter

Jay Hite
Recruiter, Account Manager

As a Recruiter at Compass, Jay enjoys meeting job seekers and helping them to find new and exciting opportunities. He enjoys the process of getting to know candidates and learning all about their experience and what their future goals are. Jay feels the excitement of his candidates and is passionate about helping to find a fit both culturally and professionally. 

When Jay isn’t working, he enjoys bike rides, trying out new foods, tequila tasting and watching movies.  

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About Brisbane, CA

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