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Metro location and 3–6 year mid-level requirement yield moderate candidate density for niche clinical programming roles.
Clinical trial SDTM/ADaM expertise is highly industry-specific, limiting cross-industry transferability.
Requires mandatory ADaM/SDTM pharmaceutical statistical programming experience plus explicit three-year minimum, narrowing candidate pool.
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Develop primary statistical programs to generate deliverables aligned with TFL shells and dataset specifications.
Validate and ensure quality and timely delivery of statistical programming outputs across assigned studies or projects.
Create and maintain study, project, or global macros and contribute to programming dataset specifications and SP standards development.
At least 3 years of statistical programming experience, preferably in pharmaceutical or device industry.
Experience with data standards such as SDTM, ADaM datasets (ADSL, ADAE, ADVS, ADQS, ADLB), TLFs, and programming deliverables.
Ability to work under general supervision and meet delivery timelines to avoid delays or errors affecting submissions.
Work hours: 1 PM to 10 PM IST; Relocation assistance provided.
Experienced in pharmaceutical/device industry statistical programming with strong knowledge of data standards and regulatory compliance.
Able to manage multiple tasks effectively and maintain quality under moderate supervision.
Capable of contributing to process improvements and working collaboratively within a statistics programming team.