Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Statistical Programmer

Navitas Life Sciences
Navitas Life Sciences
10+ years
Not Disclosed
10 May 28, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Senior Statistical Programmer


Job Overview

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


Key Responsibilities

  • Independently perform SAS programming and analysis for generation of analysis datasets, statistical analyses, listings, figures, and tables

  • Develop SAS application code independently

  • Validate SAS programs and deliverables independently

  • Perform migrations and verifications independently

  • Perform SDTM and ADaM mapping independently

  • Generate SDTM and ADaM deliverables

  • Generate all necessary output for statistical appendices related to CTR, ISS, and ISE

  • Generate data files and output for safety updates, publications, and meeting presentations

  • Interface with cross-functional client teams and DataCeutics team members

  • Act as an expert in areas such as Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries, or other domains


Desirable Skills and Experience

  • Background in statistics and statistical analysis (desirable)

  • 10+ years of 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 standards

  • Expert knowledge of SAS-based statistical programming

  • Proficiency in SAS programming across multiple platforms (Windows, UNIX, etc.) is desirable