Pr Statistical Programmer

Overview

Lead statistical programming activities for clinical trial projects, producing and validating analysis outputs and datasets using SAS or other required software. Provide technical expertise across CDISC standards, regulatory requirements, project delivery, and programmer mentoring.

What you'll do

• Develop SAS or other programming code for tables, listings, graphs, and derived datasets.
• Validate programming outputs and resolve discrepancies with project teams.
• Lead programming activities and monitor deliverables from other programmers.
• Develop specifications for datasets and outputs of varying complexity.
• Manage timelines and deliverables across multiple concurrent projects.
• Review clinical programming documentation and provide technical feedback.
• Mentor programming personnel and contribute to training.

What you'll need

• Undergraduate degree in a scientific or statistical discipline, or equivalent education and programming experience.
• Extensive SAS or other required software programming experience.
• Experience leading multiple complex or global clinical trial projects.
• Knowledge and experience using CDISC Standards for regulatory requirements.
• Excellent written and verbal communication skills.
• Ability to read, write, speak, and understand English.

Nice to have

• Experience in clinical trial programming.
• Experience with regulatory agency submissions.
• Experience mentoring others in clinical trial processes and CDISC Standards.

Details

• Remote location in India.
• Minimal travel may be required.