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Assoc. Principal Stat Programmer

10+ years
₹28,00,000 – ₹38,00,000 per annum
10 Aug. 5, 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

Associate Principal Statistical Programmer
Location: Thāne, India
Work Mode: Full-Time, Home-Based
Requisition ID: R1480445

Job Overview:
IQVIA is actively seeking an Associate Principal Statistical Programmer with deep expertise in oncology/immunology studies to lead complex programming efforts. This role demands a high level of proficiency in ADaM and TFL programming, with specific hands-on experience in efficacy endpoints and advanced visualizations. The ideal candidate will contribute to global studies in Phases II and III, playing a key role in clinical development analytics and regulatory submissions.

Key Responsibilities:

  • Lead and execute ADaM and TFL programming for oncology and immunology clinical trials

  • Develop efficacy ADaMs including:

    • ADTTE datasets for Progression-Free Survival (PFS), Overall Survival (OS), Duration of Response (DOR), Best Overall Response (BOR), and Overall Response Rate (ORR)

  • Create and validate complex visualizations such as:

    • Kaplan-Meier (KM) plots

    • Waterfall plots

    • Forest plots

  • Collaborate with cross-functional teams including statisticians, data managers, and medical writers

  • Ensure compliance with CDISC (SDTM & ADaM) standards and regulatory requirements

  • Contribute to programming best practices and mentoring junior team members

  • Participate in programming strategy, review specifications, and deliver quality outputs under tight timelines

Required Qualifications:

  • 10+ years of experience in statistical programming within clinical trials

  • Proven expertise in ADaM dataset programming and TFL generation

  • Advanced experience with oncology/immunology studies is mandatory

  • Proficiency in efficacy endpoints and their representation in datasets and plots

  • Expert in SAS programming and CDISC standards

  • Experience with Phase II and Phase III trials

  • Strong communication skills and ability to work independently in a global matrix environment

Estimated Salary: ₹28,00,000 – ₹38,00,000 per annum (based on experience and domain expertise)

About IQVIA:
IQVIA is a world leader in using data, technology, advanced analytics, and human insight to help healthcare clients drive innovation. Join our team to make a global impact in the development of life-saving treatments.

Apply Now at IQVIA Careers