Principal Statistical Data Science

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Location: Chennai (

Chennai Base Candidate ) | 🏢

Employment Type: Full-time

About the Role We are seeking a

Principal Statistical Programmer (

PSDS )to support clinical studies, projects, and data standards initiatives through high-quality statistical programming. This individual contributor role combines hands-on programming expertise with study leadership, stakeholder collaboration, and mentoring responsibilities. The ideal candidate will have strong experience in clinical trials, CDISC standards, and SAS programming, with the ability to deliver accurate, compliant, and timely results in a global environment.

What You'll Do

• Lead and deliver statistical programming activities across studies, projects, and standards initiatives.
• Develop, validate, and review SDTM/ADaM datasets, Tables, Listings, and Figures (TLFs) in accordance with CDISC and regulatory requirements.
• Program and support clinical deliverables using

SAS , with exposure to

R and/or Python considered an advantage.

• Collaborate with statisticians, clinicians, data managers, and global study teams to ensure milestone achievement.
• Maintain high-quality documentation, validation, and QC processes throughout the study lifecycle.
• Contribute to standards development, process improvements, automation initiatives, and best practices.
• Mentor junior programmers and provide technical guidance where needed.
• Support resource planning, study timelines, and departmental initiatives.

What You'll Bring

• Bachelor's degree in Statistics, Computer Science, Engineering, Pharmacy, Life Sciences, IT, or a related discipline; Master's degree preferred.
• 5+ years of statistical programming experience within the pharmaceutical MNC, biotechnology, CRO, or regulatory environment.
• Strong hands-on experience with

SAS and a solid understanding of clinical trial data and drug development processes.

• Knowledge of

CDISC standards (SDTM/ADaM) and regulatory guidelines, including ICH.

• Experience developing and reviewing datasets, TLFs, and submission-ready deliverables.
• Ability to manage multiple priorities and work independently in a fast-paced, global environment.
• Strong analytical, problem-solving, communication, and stakeholder management skills.
• Knowledge of at least one therapeutic area is preferred.

Why Join Us?

• Opportunity to work on innovative clinical development programs.
• Exposure to global teams and cutting-edge technologies.
• Collaborative environment that supports learning, growth, and career advancement.
• Meaningful contribution to improving patient outcomes through data-driven insights.

Apply today and help shape the future of clinical research through excellence in statistical programming.