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Sr. Statistical Programmer

6+ years
Not Disclosed
10 April 29, 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

Sr. Statistical Programmer
Location: Bengaluru, India
Job Type: Full Time
Job ID: R1480350

Job Description

IQVIA is seeking an experienced Sr. Statistical Programmer with strong expertise in ADaM and TFL programming. This role requires a proven background in Oncology or Immunology studies, specifically in handling efficacy data sets and advanced statistical graphics. Ideal candidates will be adept in generating and validating complex datasets and visual outputs in accordance with industry standards and study protocols for Phases 2 and 3 clinical trials.


Key Responsibilities

  • Program and validate ADaM datasets and TFLs with a focus on Oncology/Immunology efficacy endpoints.

  • Deliver efficacy datasets such as ADTTE supporting PFS, OS, DOR, BOR, and ORR.

  • Generate and validate advanced graphical outputs including Kaplan-Meier plots (KM Plots), waterfall plots, and forest plots.

  • Collaborate with statisticians, data managers, and other programming team members to meet project goals.

  • Ensure compliance with CDISC standards and regulatory guidelines in all deliverables.

  • Participate in code reviews, quality checks, and documentation of programming activities.

  • Handle multiple programming assignments in a fast-paced, deadline-driven environment.


Qualifications

  • Education: Bachelor’s or Master’s degree in Statistics, Computer Science, Life Sciences, or a related field.

  • Experience:

    • Minimum 6+ years of hands-on experience in clinical trial statistical programming.

    • Proficient in ADaM and TFL programming for Phase 2 and 3 clinical trials.

    • Solid experience with efficacy datasets and programming for Oncology/Immunology studies.

  • Technical Skills:

    • Expertise in SAS programming.

    • Experience in generating KM plots, waterfall plots, and forest plots.

  • Strong problem-solving skills, attention to detail, and the ability to work both independently and within a team.


About IQVIA
IQVIA is a world-leading provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We connect data, insights, and innovation to drive better healthcare decisions and outcomes. Learn more at
IQVIA Careers.

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