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Assoc. Principal Stat Programmer

10+ years
Not Disclosed
10 Nov. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Associate Principal Statistical Programmer

Location: Thane, India | Job ID: R1480445 | Full-Time | Home-Based | Additional Locations Available

Position Overview

IQVIA is seeking a highly experienced Associate Principal Statistical Programmer to lead advanced statistical programming activities across global clinical studies. This senior-level role focuses on ADaM datasets, TFL development, and complex oncology/immunology efficacy analyses. The position requires strong technical leadership, domain expertise, and the ability to independently deliver high-quality statistical programming outputs in a remote/home-based environment.


Key Responsibilities

  • Develop, validate, and review ADaM datasets and TFLs for complex clinical studies.

  • Lead programming activities in Oncology and Immunology therapeutic areas with emphasis on efficacy endpoints including:

    • ADTTE, PFS, OS, DOR, BOR, ORR

  • Create advanced visualizations such as Kaplan–Meier (KM) plots, waterfall plots, and forest plots.

  • Ensure high-quality statistical outputs for Phase II and Phase III clinical trials.

  • Collaborate with cross-functional teams including Biostatistics, Clinical, and Project Management.

  • Ensure adherence to industry standards, regulatory guidelines, and IQVIA programming processes.

  • Support project timelines, quality checks, and delivery milestones in a fast-paced environment.


Experience Required

  • Minimum 10+ years of hands-on experience in SAS statistical programming.

  • Extensive expertise in ADaM programming and TFL development is mandatory.

  • Strong background in Oncology/Immunology clinical studies focused on efficacy analyses.

  • Proven experience with:

    • ADTTE datasets (PFS, OS, DOR, BOR, ORR)

    • KM plots, waterfall plots, and forest plots

  • Prior experience in Phase II and Phase III clinical trials is preferred.

  • Ability to work independently in a remote environment with high attention to detail and data quality.


About IQVIA

IQVIA is a global leader in clinical research, real-world evidence, commercial insights, and healthcare intelligence. With advanced analytics, technology, and scientific expertise, IQVIA accelerates the development of innovative medical treatments and improves patient outcomes worldwide.


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