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Metro location and reputable CRO increase applicants, but niche clinical SAS/R skillset limits density.
High — clinical trial statistical programming skills are specialized and not easily transferable outside biopharma.
Requires clinical SAS/R expertise, regulatory (ICH/GCP) knowledge and leadership, so moderate strictness.
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Lead and manage a team of statistical programmers to deliver accurate statistical analysis outputs for clinical trials.
Oversee development, validation, and maintenance of statistical programs (SAS, R, or similar) ensuring adherence to clinical research standards.
Manage project timelines, quality control, and collaborate with stakeholders including biostatisticians and project managers.
Bachelor's degree in statistics, computer science, mathematics, or related field.
Significant experience in statistical programming within clinical research, with strong understanding of statistical methodologies.
Proven leadership experience managing teams and delivering projects in fast-paced environments.
Proficiency in SAS, R, or Python programming languages and experience with clinical data management systems.
Experienced leader capable of managing competing priorities and developing team capability in statistical programming.
Skilled in cross-functional collaboration with stakeholders like biostatisticians and project managers in clinical trial settings.
Comfortable operating within regulated environments following ICH/GCP guidelines and driving continuous process improvements.