Senior Statistical Programmer Analyst - T

Your Remote US Home Officefull time

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Remote

senior

H1B: no

Penumbrainc Senior Statistical Programmer Analyst at Penumbra develops analysis programs to support clinical data statistical analysis under general supervision. The role includes preparing datasets, producing data listings, and mentoring less experienced programmers.

Responsibilities

Develop algorithms and write programs to create datasets following specifications
Produce data listings, summary tables and graphs using analysis software
Independently check data listings, summary tables and graphs
Import and export data
Assist data management group in performing data edit checks
Maintain understanding of CDISC guidance documents and FDA regulations
Prepare clinical trial datasets and programs for regulatory submission
Write specifications for analysis datasets following statistical analysis plan
Interact with project statisticians and other programmers
Manage the data warehouse for clinical study data libraries
Interact with regulatory affairs, quality assurance staff, and external vendors
Mentor less experienced statistical programmers

Qualification

Bachelor's degree in StatisticsFamiliarity with Base SASProven ability to handle multiple tasksKnowledge of international regulations

Required

Bachelor's degree in Statistics, Computer Science or related field
5+ years of statistical programming experience
3+ years of clinical statistical programming experience in medical device or related industry
Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, and SAS/STAT

Preferred

•Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, and SAS/STAT
•SAS Certified Base and/or Advance Programmer experience is preferred
•Experience with macro programming and SAS/SQL a plus
•Proven ability to handle multiple tasks
•Able to identify ways to improve business performance and campaigning for it when necessary
•Knowledge of international regulations, requirements and guidance associated with clinical data standards and clinical databases used for regulatory submission
•Knowledge of clinical data standards including CDASH, SDTM, ADaM, SHARE, BRIDG, ODM, Define and controlled terminology
•Experience with metadata repository in clinical data a plus

Benefits

Vision

Company

Penumbrainc

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Source: lever

Active within the past hour

Remote-friendly

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