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Mid-level (3–5 years) metro role with common SAS and clinical requirements increases applicant competition.
High because clinical trials, GxP compliance and SAS expertise limit cross-industry transferability.
Explicit 3–5 years, required SAS/GxP experience and clinical/regulatory skills make filters stringent.
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Develop and validate custom programming reports using SAS to support clinical data cleaning and ensure data integrity throughout multiple clinical projects.
Collaborate cross-functionally with R&D teams, Biostatisticians, and external partners to meet clinical data management deliverables and maintain compliance with GxP regulations.
Manage project schedules, communicate programming progress, and contribute to regulatory submission drafting and audit processes.
Bachelor's or Master's degree in related fields.
3-5 years of relevant experience, preferably including vaccine development experience.
Expertise in SAS programming with basic and advanced certifications.
Strong knowledge of GxP standards including GLP, GCP, and GMP.
Experienced in clinical trial data management and electronic data capture systems relevant to animal/human health R&D.
Proficient in managing multiple projects with shifting priorities and timelines within regulated environments.
Capable of clear and impactful technical communication tailored to diverse audiences including regulatory authorities.