Senior Clinical SAS Programmer & CDISC SME

Penumbra, Inc.; Kansas; Hybrid; USD 90,000 - 158,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) with employer match

Paid parental leave

Paid holidays

Vacation accrual

Job summary

Penumbra, Inc. is seeking an experienced Statistical Programmer to support the preparation and statistical analysis of clinical data for trials.

You will develop SAS programs, create datasets, listings, tables and graphs, and collaborate with biostatisticians and data managers to ensure regulatory submission readiness. The role involves mentoring junior programmers, maintaining CDISC guidance, and ensuring adherence to GCP, 21 CFR Part 11, and internal SOPs.

Qualifications

• Bachelor's degree in Statistics, Computer Science or related field with 5+ years of statistical programming experience with 3+ years in clinical statistical programming within medical device or related industry (biotechnology, pharmaceutical, Clinical Research Organization) or equivalent combination of education and experience

Responsibilities

• Following specifications, develops algorithms and writes programs to create datasets.
• Produces data listings, summary tables and graphs using analysis software.
• Independently checks data listings, summary tables and graphs.
• Imports and exports data.
• Assists data management group in performing data edit checks to facilitate data cleaning.
• Prepares clinical trial datasets and programs for regulatory submission.
• Interacts with the project statistician and other programmers participating on a project team.
• Mentors less experienced statistical programmers.
• Act as the subject matter expert on CDISC and good statistical programming practices.

Skills

Base SAS

SAS/GRAPH

SAS/ODS

SAS/STAT

SAS MACROS

SAS/SQL

Data analysis

Data import/export

CDISC/SDTM/ADaM

Education

Bachelor's degree in Statistics/CS or related field

Tools

Oracle InForm

RAVE

Job description

Penumbra, Inc. is seeking an experienced Statistical Programmer to support the preparation and statistical analysis of clinical data for trials.

You will develop SAS programs, create datasets, listings, tables and graphs, and collaborate with biostatisticians and data managers to ensure regulatory submission readiness. The role involves mentoring junior programmers, maintaining CDISC guidance, and ensuring adherence to GCP, 21 CFR Part 11, and internal SOPs.