Pr. Statistical Programmer (Clinical Pharmacology)

Overview

Lead statistical programming for clinical pharmacology, using SAS to produce and validate clinical trial outputs and ensure quality and compliance. Coordinate programming timelines, manage documentation, and represent statistical programming in sponsor-facing meetings.

What you'll do

• Develop custom SAS programming code to generate summary tables, data listings, graphs, and derived datasets per the statistical analysis plan.
• Ensure outputs meet quality standards and project requirements.
• Perform validation programming and resolve discrepancies with biostatisticians and programming team members.
• Maintain programming progress communications and manage concurrent deliverables for on-time delivery.
• Oversee validation/quality control documentation and maintain inspection-ready project documentation.
• Lead programming activities, review key documents, and provide feedback to reduce inefficiencies.
• Serve as CDISC technical subject matter expert and perform compliance reviews for CDISC deliverables.

What you'll need

• Extensive SAS (or other required software) programming experience, preferably in a clinical trial environment.
• Knowledge and experience with CDISC standards for regulatory agency requirements.
• Experience leading multiple complex and/or global projects with teams of statistical programmers.
• Possess an undergraduate degree, preferably in a scientific or statistical discipline (or an equivalent combination of education and programming experience).
• Strong written and verbal communication skills.
• Ability to read, write, speak, and understand English.

Details

• Location: IND-Hyderabad.
• Minimal travel may be required.