Sr. Statistical Programmer with SDTM / Metadata management specialization

Overview

Lead statistical programming activities for clinical trial projects, specializing in SDTM and metadata management. Develop, validate, and review programming deliverables while coordinating with project teams and sponsors.

What you'll do

• Develop SAS or other programming code for tables, listings, graphs, and derived datasets.
• Perform validation programming and resolve discrepancies with project team members.
• Develop dataset and output specifications based on statistical and sponsor requirements.
• Lead programming activities and monitor other programmers' deliverables.
• Review statistical analysis plans, mock shells, programming specifications, annotated CRFs, and database designs.
• Maintain project documentation, testing, and quality control records.
• Participate in sponsor, kickoff, and bid defense meetings as required.

What you'll need

• Undergraduate degree, preferably in a scientific or statistical discipline, or equivalent education and programming experience.
• Extensive programming experience in SAS or other required software.
• Clinical trial programming experience is preferred in the qualifications.
• Excellent written and verbal communication skills.
• Ability to read, write, speak, and understand English.
• Ability to direct programming personnel and monitor deliverables.

Details

• Location: Hyderabad, India.
• Work mode: Hybrid.
• Minimal travel may be required.