Senior Statistical Programmer

Senior Statistical Programmer / Principal Statistical Programmer

Location: Bangalore

Employment Type: Full-time

Hiring Type:

Immediate Hiring Immediate Joiners Preferred

Job Overview:

We are looking for experienced Senior / Principal Statistical Programmers to support clinical studies and regulatory submissions. The ideal candidate will have strong expertise in SAS programming, CDISC standards, and hands-on experience working with clinical trial data.

Key Responsibilities:

• Develop, validate, and maintain ADaM analysis datasets, tables, figures, and listings (TFLs) for clinical studies and regulatory submissions
• Design and implement complex SAS programs for data extraction, transformation, analysis, and reporting of clinical trial data
• Ensure submission readiness and data quality in compliance with CDISC standards (SDTM, ADaM, define.xml)
• Lead and support Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE), including pooled and exploratory analyses
• Provide programming support for regulatory responses, safety analyses, publications, and presentations

Required Skills:

• Strong hands-on experience in SAS programming
• In-depth knowledge of CDISC standards (SDTM & ADaM)
• Experience in clinical trial data analysis and regulatory submissions
• Basic to intermediate knowledge of R programming
• Strong analytical and problem-solving skills

Important Notes:

• Candidates must currently be based in the specified location profiles from other locations will not be considered
• This is an urgent requirement, so only immediate or short notice joiners should apply
• Shortlisted candidates will be invited for a 15-minute screening call via Microsoft Teams before further client submission

How to Apply:

Interested candidates can share their updated resume at the earliest.

Apply now to be part of a fast-moving clinical programming team working on global regulatory submissions.