Senior Clinical SAS Programmer & CDISC Data Specialist

Penumbra; Alameda (CA); Remote; USD 90,000 - 158,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Life insurance

AD&D, disability insurance

401(k) with employer match

Parental leave

Holidays and vacation

Job summary

Penumbra, Inc. in Alameda, California, seeks a Statistical Programmer to develop analysis programs for clinical data, create datasets, and produce listings, tables and graphs under supervision.

You will collaborate with biostatisticians and clinical data managers on trials and regulatory submissions. Role requires 5+ years of clinical statistical programming experience, strong SAS and macro skills, and familiarity with CDISC standards; travel minimal and adherence to QMS essential.

Qualifications

• Bachelor's degree in Statistics, CS, or related field with 5+ years of statistical programming experience in medical device or related industry.
• Experience with CDISC standards (CDASH, SDTM, ADaM) is preferred.
• SAS programming expertise including macro development and data manipulation.

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.
• Mentors less experienced statistical programmers.
• Builds efficient SAS coding and macro libraries.
• Adheres to GCP, ICH, 21 CFR 11 and regulatory requirements.

Skills

Statistical programming

Multiple task management

Data analysis

SAS/macros

Education

Bachelor's degree in Statistics, Computer Science or related field

Tools

Base SAS

SAS/GRAPH

SAS/ODS

SAS/STAT

SAS/SQL

Job description

Penumbra, Inc. in Alameda, California, seeks a Statistical Programmer to develop analysis programs for clinical data, create datasets, and produce listings, tables and graphs under supervision.

You will collaborate with biostatisticians and clinical data managers on trials and regulatory submissions. Role requires 5+ years of clinical statistical programming experience, strong SAS and macro skills, and familiarity with CDISC standards; travel minimal and adherence to QMS essential.