WEP Clinical is expanding its India team and is looking for an experienced Senior Statistical Programmer to support its global Clinical Data Management & Biometrics operations.

The role will be responsible for statistical programming activities supporting clinical trials, including data preparation, analysis, reporting and regulatory submissions.

Key Responsibilities
Develop and validate SAS programs for clinical trial data analysis and reporting.
Create and work with CDISC SDTM and ADaM datasets.
Perform TLF programming and validation for clinical studies.
Support clinical trial data analysis and regulatory submission activities.
Collaborate with Biostatistics, Clinical Data Management and other cross-functional teams.
Ensure programming deliverables meet applicable quality and regulatory standards.
Contribute to programming standards, processes and documentation.





Required Skills
8+ years of experience in statistical programming within clinical research.
Solid hands-on experience with SAS programming.
Strong knowledge of CDISC SDTM and ADaM.
Experience with Tables, Listings and Figures (TLFs) and programming validation.
Experience working with clinical trial data.
Regulatory submission experience preferred.
SAS LSAF experience is an advantage.
Solid understanding of GCP and clinical research processes.

Why Join WEP Clinical?
Work on global clinical studies.
Collaborate with international clients and teams.
Be part of a growing India team.
Chance to contribute to and shape processes and ways of working.

📌 Senior Statistical Programmer, Clinical Research Bengaluru
🏢 RN Consulting
📍 Bengaluru