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Pfizer, a global leader in pharmaceuticals, is seeking a Senior Statistical Data Scientist to join their team in Chennai. This is a hybrid/flexible role, offering an excellent opportunity for professionals with expertise in SAS programming, clinical trials, and statistical data analysis.
Job Description
Key Responsibilities:
- Develop analysis-ready datasets, tables, listings, and figures for clinical study reports.
- Ensure high-quality programming standards and timely delivery of statistical outputs.
- Collaborate with statisticians and programming leads to clarify specifications.
- Maintain proper documentation and perform quality control (QC) for all programming deliverables.
- Contribute to department-level initiatives and assist in developing study-specific standards.
- Stay updated with ICH guidelines, regulatory requirements, and clinical data standards.
Qualifications & Experience:
- Bachelor’s or Master’s degree (preferred) in Statistics, IT, Biological Sciences, or related fields.
- 3+ years of experience in pharmaceuticals, biotech, CRO, or regulatory agencies.
- Strong hands-on experience in SAS programming and statistical analysis.
- Knowledge of clinical trial data operations and reporting requirements.
- Familiarity with CDISC standards (SDTM, ADaM) is a plus.
Work Location & Flexibility:
- Hybrid work model (Chennai-based with flexible remote options).
- Pfizer promotes work-life balance and equal employment opportunities.
About Pfizer
Pfizer is a world-renowned biopharmaceutical company committed to innovation, patient care, and scientific excellence. With a strong global presence, Pfizer focuses on developing breakthrough medicines and vaccines to improve lives worldwide.
Why Join Pfizer?
- Industry-leading research & development
- Collaborative and inclusive work culture
- Competitive salary & benefits
- Career growth opportunities
How to Apply
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