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Niche clinical SAS/CDISC role reduces applicants, but metro location and known CRO increase competition.
Clinical trial SAS programming and CDISC expertise have limited transferability across industries.
Mandatory clinical SAS/CDISC expertise and regulatory experience enforce strict candidate filtering.
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Develop and validate SAS programming outputs (tables, listings, graphs, datasets) per statistical analysis plans ensuring quality and regulatory compliance.
Lead and coordinate multiple concurrent programming projects, managing timelines, risks, and communication with project teams and sponsors.
Act as a technical subject matter expert on CDISC standards, providing guidance, review, and training for complex regulatory submissions.
Undergraduate degree in a scientific or statistical discipline or equivalent experience.
Extensive SAS programming experience in clinical trial environments, demonstrated by leading complex/global projects with teams.
Knowledge and experience with CDISC standards for regulatory requirements; experience in regulatory submissions preferred.
Work Experience Required: Extensive programming experience with leadership in clinical trial programming setups.
Experienced in managing end-to-end statistical programming deliverables under regulatory and industry standards in global clinical trials.
Strong leadership and coordination skills demonstrated by leading programming teams and managing multiple projects.
Deep expertise in CDISC standards and clinical drug development processes with ability to mentor others and liaise with sponsors.