Lead Sas Programmer Clinical Trials

SAS programming and clinical research expertise define this Principal Statistical Programmer role with Alira Health. Support high-quality deliverables across client projects.This position leads statistical programming activities, including complex clinical projects, while following standard operating procedures and agreed timelines. Responsibilities include CDISC dataset development, statistical analysis results, risk support, resource deployment, audits, and mentoring. Knowledge of R is a plus.Key Responsibilities:
Specify, program, and validate clinical study datasetsProgram statistical analysis results, tables, listings, and figuresIdentify scope changes and risks to contractual deliveryReport deviations, KPIs, complaints, and manage CAPAsSupport audits, training, and effective departmental maintenanceRequirements:
At least five years in statistical programmingExcellent SAS programming skills and R knowledge preferredDegree or equivalent experience in relevant quantitative disciplineStrong clinical research principles and techniques knowledgeAnalytical problem-solving and effective prioritization abilitiesUse SAS, clinical research knowledge, CDISC programming, and analytical judgment to deliver validated clinical project outputs.
#J-18808-Ljbffr