IQVIA is a premier global provider of advanced analytics, clinical research, and healthcare intelligence for the life sciences industry. With a mission to accelerate medical breakthroughs, IQVIA supports pharmaceutical companies, biotech firms, and healthcare organizations in bringing innovative treatments to market.
Job Description: Statistical Programmer
📍 Location: Thane, Maharashtra, India
📅 Job Type: Full-time
📌 Requisition ID: R1438804
Key Responsibilities:
✔ Develop SAS/R programs to generate derived analysis datasets, tables, listings, and figures (TLFs).
✔ Perform programming validation to ensure data accuracy.
✔ Support electronic submissions (e-submissions) for regulatory compliance.
✔ Review statistical analysis plans (SAP), data presentation plans (DPP), and data review plans (DRP).
✔ Collaborate with vendors, internal teams, and stakeholders on project standards.
✔ Ensure compliance with CDISC standards (SDTM, ADaM) and regulatory requirements.
✔ Improve process efficiency through automation and best practices.
Eligibility & Requirements
Minimum Qualifications:
- Bachelor’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.
- 3+ years of programming experience (SAS/R preferred).
- Knowledge of CDISC standards (SDTM, ADaM) and clinical data structures.
- Familiarity with regulatory submission requirements.
- Proficiency in MS Office, XML, and Linux (preferred).
Preferred Qualifications:
- 3+ years in clinical/statistical programming (pharma/biotech).
- Experience with R programming and Linux OS.
- Understanding of drug development, clinical trials, and regulatory guidelines.
Benefits & Why Join IQVIA?
✅ Global exposure in clinical research & healthcare analytics.
✅ Competitive salary & growth opportunities.
✅ Hybrid/remote work flexibility (if applicable).
✅ Learning & development programs.
✅ Collaborative work culture with industry experts.
How to Apply
