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Tier-1 employer and Bangalore location increase density, but SAS/CDISC niche reduces broad applicant competition.
Highly domain-specific clinical-statistics skills (SAS, CDISC) limit transferability across industries.
Mandatory SAS and CDISC/ADaM/SDTM expertise plus regulated clinical trials experience implies high shortlisting strictness.
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Lead statistical programming activities across multiple clinical trial projects, ensuring data integrity and compliance with regulatory and company standards.
Oversee and mentor junior statistical programmers, establish programming solutions and best practices to support clinical trial data analysis.
Collaborate cross-functionally to align programming tasks with project timelines and contribute to strategic planning for process improvements.
Bachelor's degree in Statistics, Computer Science, or related field mandatory; Master's preferred.
Proven expertise in SAS programming and knowledge of CDISC standards (ADaM, SDTM).
Experience working in regulated environments supporting clinical trials.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in leading and managing statistical programming teams within clinical research settings.
Skilled at navigating regulatory requirements and ensuring high-quality deliverables under tight deadlines.
Capable of cross-department collaboration and strategic contribution to programming methodologies and operational efficiency.