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Tier-1 brand and metro location increase competition, but niche SAS/statistical programming moderates density.
Clinical statistical programming and regulatory knowledge make background highly industry-specific.
Explicit 5–8 years requirement and mandatory SAS/statistical programming skills enforce strict shortlisting.
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Design, develop, and implement technical solutions for clinical data integration, analysis, and reporting to support drug development and regulatory approval.
Provide comprehensive programming support including strategy, standards, and specifications for clinical project teams and external vendors.
Contribute to process improvement, standardization, and quality assurance of deliverables adhering to regulatory requirements and corporate SOPs.
5 - 8 years clinical/statistical programming experience within pharmaceutical clinical development.
Undergraduate or Graduate degree in statistics, biostatistics, mathematics, computer science or equivalent experience preferred.
Significant knowledge of SAS software (Base, Stat, Graph) and understanding of clinical trial methodology and global regulatory requirements.
On-site presence required as per Site-essential or Site-by-design occupancy structure (minimum 50% onsite if hybrid).
Experienced in oncology clinical trials programming preferred.
Strong technical expertise in SAS programming applied to clinical drug development.
Skilled at collaborating across cross-functional teams and interfacing with external vendors to meet project and regulatory objectives.