Senior Statistical Programmer, Clinical Research

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.
• Strong 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.
• Strong 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.
• Opportunity to contribute to and shape processes and ways of working.