IQVIA

Principal Statistical Programmer

IQVIA
Bengaluru/Bangalore
Not disclosed
Work from OfficeWork from Office
Full TimeFull Time
Min. 10 yearsMin. 10 years

Job Description

Principal Stat Programmer

We are seeking highly experienced Statistical Programmers with a minimum of 10+ years of hands-on experience in ADaM and TFL programming, with strong exposure to R programming.

Key Responsibilities & Experience Requirements

  • Extensive experience in Efficacy ADaMs and TFL development, particularly within Oncology and Immunology studies
  • Strong expertise in Oncology efficacy endpoints, including:
    • ADTTE-based analyses such as PFS, OS, DOR, BOR, and ORR (mandatory)
  • Proven experience supporting Phase II and Phase III clinical studies (preferred)
  • In-depth knowledge of Oncology efficacy ADaM datasets, including:
    • ADTR, ADRS, ADQS, ADTTE
  • Experience with Non-Oncology efficacy datasets, including:
    • ADEFF, ADQS
  • Working knowledge of PK/PD datasets used for pharmacokinetic and pharmacodynamic analyses, including:
    • ADPD, ADPC, ADPK, ADPP
  • Strong experience creating Oncology statistical outputs and visualizations, including:
    • Kaplan–Meier (KM) plots
    • Forest plots

Statistical & Programming Expertise

  • Hands-on experience with key SAS statistical procedures, including:
    • PROC LIFETEST
    • PROC PHREG
    • PROC MIXED
  • Ability to work independently on complex programming deliverables while adhering to regulatory and quality standards

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Experience Level

Senior Level

Job role

Work location
Work locationBangalore, India
Department
DepartmentResearch & Development
Role / Category
Role / CategoryPharma & Biotech Research
Employment type
Employment typeFull Time
Shift
ShiftDay Shift

Job requirements

Experience
ExperienceMin. 10 years

About company

Name
NameIQVIA
Job posted by IQVIA

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