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Senior niche SAS/CDISC role and 10+ years seniority limit applicant pool.
Clinical SAS and CDISC expertise is industry-specific, limiting cross-industry transferability.
Explicit 10+ years and mandatory SAS/CDISC expertise plus leadership make filters strict.
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Design, develop, and validate SAS programs for statistical analysis and reporting of clinical trial data.
Lead programming teams, manage study deliverables across Phases I–IV clinical trials, and ensure compliance with regulatory guidelines.
Mentor junior programmers and collaborate with biostatisticians on analysis plans and statistical methods.
10+ years of Clinical Programming experience with strong expertise in SAS.
Expert knowledge of CDISC SDTM standards, LSAF, clinical data review, data transformations, and regulatory deliverables.
Proven leadership experience managing programming teams and study deliverables in clinical trials.
Employment contingent on legal right to work in the country of the role.
Experienced in leading and delivering programming activities for global regulatory submissions in clinical development programs.
Skilled in developing macros, edit checks, visualizations, and submission packages for regulatory agencies.
Effective collaborator able to manage multiple priorities and guide teams toward compliant, high-quality results.