Senior Statistical Programmer with R

Role overview

Experience and qualifications

• Requires 7–10 years of experience; the posting also lists 5 years as a statistical programmer as required.
• Candidates must have hands-on ADaM and TFL programming experience covering safety and efficacy.
• Strong CDISC and regulatory-framework knowledge, including GCP and ICH, is required.
• Quality delivery, team coordination, communication, and collaboration are required.
• R programming experience is preferred.

Responsibilities

• Contribute to or lead statistical programming for Phase I–IV clinical trials.
• Develop and validate datasets, tables, listings, and figures to specifications.
• Coordinate with biostatistics, data management, and clinical teams; communicate progress and issues.
• Follow CDISC SDTM/ADaM, GCP, and other company, departmental, and industry standards.
• Maintain audit readiness and regulatory compliance; review or develop analysis-plan programming specifications.
• Review eCRFs and data structures; check deliverable accuracy, reliability, and quality.
• Use SAS and other statistical programming tools, including R.
• Mentor junior programmers and improve and standardize processes.
• Coordinate study-level programming and deliver milestones such as DMCs, interim analyses, publications, CSRs, and submissions on time.

Compensation and benefits

• Pay is ₹2,000,000–₹2,500,000 per year.
• Provident Fund is listed as a benefit.