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Principal Statistical Programmer
IQVIA India
PAN India
Not Disclosed
10 - 16 Years
Full Time - Permanent
Views:1
Applicants:0
Posted on 26 Aug, 2026
In Office
Job Description | Responsibilities
- Lead statistical programming for complex clinical trials using SAS and related tools.
- Develop and validate SDTM, ADaM datasets, Tables, Listings, and Figures (TLFs).
- Ensure CDISC, FDA, ICH-GCP, and regulatory submission compliance.
- Provide technical leadership, QC, mentoring, and cross-functional project coordination.
- Support regulatory submissions, documentation, programming standards, and process improvements.
Overview
- Industry - MEDICAL / HEALTHCARE / HOSPITALS
- Job Role - Principal Statistical Programmer
- Employment type - Full Time - Permanent
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
SAS
Clinical Trials
SDTM
ADaM
CDISC
TLF
Statistical Programming
FDA
ICH-GCP