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Pfizer brand, Chennai metro and mid-level title increase competition, but niche clinical SAS statistical skills narrow the pool.
Clinical-trials, SAS statistical programming, and regulatory standards make skills highly industry-specific to pharma/CRO.
Mandatory 3+ years, SAS/statistical programming and clinical trials/regulatory expertise make shortlisting highly selective.
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Deliver statistical programming outputs including analysis ready datasets, tables, listings, and figures to support clinical study reports and asset level deliverables.
Ensure high quality programming standards, appropriate documentation, and quality control throughout the study lifecycle.
Collaborate with statisticians and programming leads to clarify specifications and apply knowledge of core safety and therapeutic area standards.
Bachelor or Master degree in Statistics, Biological Sciences, IT, or related field.
At least 3 years of relevant experience in pharmaceutical, biotech, CRO, or Regulatory Agency.
Hands-on experience in Statistical Programming with SAS.
Knowledge of clinical trials data operations, ICH, regulatory guidelines, and clinical data standards.
Experienced in programming complex clinical trial datasets with strong attention to detail and quality control.
Able to work independently with limited supervision and manage timely delivery of outputs.
Capable of collaborating effectively with statisticians and programming leads, contributing to department initiatives and possibly developing standards.