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Assoc. Principal Stat Programmer

Iqvia
IQVIA
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.


Apply Now

Advance your career by contributing to impactful global clinical research programs.