Senior Statistical Programmer

Navitas Life Sciences

$100K — $130K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 10+ years of experience in Pharmaceutical or CRO industry
  • Expert knowledge of SAS programming including SAS/Base, SAS/Macro, and SAS/STAT
  • Working knowledge of CDISC, SDTM, and ADaM standards
  • Strong background in statistics and statistical analysis
  • Proficiency in SAS programming across various platforms including Windows and UNIX.

Responsibilities

  • Perform SAS programming and analysis to generate datasets and statistical outputs
  • Develop SAS application code independently for various reporting needs
  • Validate SAS programs and deliverables to ensure accuracy
  • Execute migrations and verifications as part of the programming process
  • Map SDTM and ADaM datasets accurately
  • Generate statistical appendices for clinical trial reports
  • Produce output for safety updates, publications, and presentations
  • Act as an expert in specialized areas such as Project Management and SAS programming.

Benefits

  • Opportunities for professional development and training
  • Collaborative team environment with cross-functional interactions
  • Exposure to diverse clinical projects within the pharmaceutical industry
  • Chance to be recognized as an expert in specific programming areas
  • Access to advanced tools and technologies in statistical programming.
Full Job Description
Job Description

The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory submissions and publications.

Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification and submissions support.

About the Role

  • Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures and tables;
  • Independently, develop SAS application code;
  • Independently, perform validation of SAS programs and deliverables;
  • Independently, perform migrations and verifications;
  • Independently, perform SDTM and ADaM mapping;
  • Generate SDTM and ADaM deliverables;
  • Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and ISE;
  • Generate data files and/or output for safety updates, publications and meeting presentations;
  • Interface with a cross-function of client and DataCeutics team members; and
  • Act as an Expert in one or more areas that may include Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries or other areas.


Desirable Skills and Experience

  • Background in statistics and statistical analysis is desirable
  • 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming
  • Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming
  • Working knowledge of CDISC, SDTM and ADaM
  • Expert knowledge of SAS-based statistical programming
  • Proficiency in SAS programming on multiple platforms and operating systems, e.g. Windows, UNIX, etc. is desirable

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