Assoc principal Stat Programmer -FSP

IQVIA India; India; On-site; INR 4,000,000 - 7,000,000; Full time

Job summary

IQVIA India is seeking a highly experienced Senior/Lead Statistical Programmer to lead ADaM and TFL programming for oncology/immunology efficacy analyses. The role requires hands-on experience with ADTTE datasets and time-to-event analyses, plus leadership and strong SAS/R skills.

Location: PAN India. You will collaborate with statisticians, data management, and clinical teams to deliver regulatory-compliant outputs for Phase II/III studies.

Qualifications

• 10+ years of experience in statistical programming within pharma, CRO, or biotech.
• Strong expertise in ADaM and TFL programming.
• Proven hands-on experience in Oncology and/or Immunology efficacy analyses.
• Experience with ADTTE datasets and time-to-event analyses.
• Minimum 2 years of lead or study-level programming experience.
• At least 1 year of hands-on R programming experience.
• Solid experience on Phase II and Phase III clinical studies.
• Advanced proficiency in SAS (Base, Macros; additional SAS tools).

Responsibilities

• Lead and manage statistical programming activities for Phase II/III studies.
• Collaborate with statisticians, data management, and clinical teams to ensure regulatory-compliant outputs.
• Mentor junior programmers and ensure timely, accurate deliverables.
• Develop complex efficacy graphics and ADaM datasets to support analyses.

Skills

ADaM programming

TFL programming

Oncology analyses

Immunology analyses

ADTTE datasets

R programming

Time-to-event

Leadership

SAS programming

Tools

SAS

R

Job description

Job title : Assoc principal Stat Programmer - FSP

Experience: 10+ Years

Therapeutic Focus: Oncology / Immunology/Neuroscience

Study Phase: Phase II & Phase III

Location: PAN India

Job Overview:

We are seeking a highly experienced Senior/Lead Statistical Programmer with strong expertise in ADaM and TFL programming, and deep hands‑on experience in Oncology and/or Immunology efficacy analyses. The ideal candidate will have proven capability in ADTTE datasets, advanced efficacy endpoints, and generation of complex statistical graphics, along with leadership experience and hands‑on R programming skills.

This role requires close collaboration with statisticians, data management, and clinical teams to deliver high-quality, regulatory-compliant outputs for Phase II and Phase III clinical studies.

Required Qualifications & Experience

• 10+ years of experience in statistical programming within the pharmaceutical, CRO, or biotech industry
• Strong expertise in ADaM and TFL programming
• Proven hands‑on experience in Oncology and/or Immunology efficacy analyses
• Extensive experience with ADTTE datasets and time-to-event analyses
• Minimum 2 years of lead or study-level programming experience
• At least 1 year of hands‑on R programming experience
• Solid experience working on Phase II and Phase III clinical studies
• Advanced proficiency in SAS (Base, Macros; additional SAS tools as applicable).