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Principal Stat Programmer

10-11 years
Not Disclosed
10 Feb. 12, 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

Job Title: Principal Stat Programmer
Location: Hyderabad, India
Job Type: Full-time
Job ID: R1455821

Job Overview:

IQVIA is looking for a Principal Stat Programmer with extensive experience in ADaM and TFL programming, particularly in Oncology studies. You will be responsible for generating ADaM datasets and TFLs for efficacy analysis, including key metrics such as PFS, OS, DOR, BOR, and ORR. You will also be involved in the creation of plots (e.g., KM Plots, Waterfall Plots, Forest Plots) for clinical studies, particularly in Phase 2/3 trials.

Key Responsibilities:

  • Develop ADaM datasets and TFLs (Tables, Figures, Listings) for Oncology studies, with a focus on efficacy endpoints.
  • Implement and produce ADTTE datasets for PFS, OS, DOR, BOR, and ORR.
  • Generate statistical plots, including Kaplan-Meier (KM) plots, waterfall plots, and forest plots.
  • Collaborate with the clinical and biostatistics teams to ensure the quality and consistency of statistical analysis.
  • Handle complex programming tasks and ensure compliance with relevant clinical research standards and guidelines.
  • Lead and mentor junior programmers on statistical programming activities.

Qualifications:

  • Minimum of 10+ years experience in statistical programming, particularly with ADaM and TFL programming.
  • Experience in Oncology studies, with a strong understanding of key efficacy endpoints (PFS, OS, DOR, BOR, ORR).
  • Hands-on experience with KM plots, waterfall plots, and forest plots.
  • Preferably, experience working in Phase 2/3 clinical trials.
  • Expertise in SAS programming and knowledge of statistical methods for clinical trials.
  • Strong problem-solving, organizational, and communication skills.

About IQVIA:

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. The company connects innovative treatments with the market, improving patient outcomes and advancing healthcare worldwide.

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For more details, visit IQVIA Jobs.