Lead Clinical SAS Programmer

Responsibilities:

• Plan and manage programming activities across multiple studies to deliver all data analysis outputs to agreed timelines and quality, (e.g., analysis datasets, tables, figures and listings for regulatory submissions and publications).
• Oversee outsourced tasks to third party vendors to meet the agreed timelines, quality and budget requirements established for the project or study.
• Implement data standards within a function, or therapeutic area in accordance with industry standards
• Review and inputs in eCRF desigining.
• Collaborate effectively with internal and external teams to support and resolve the programming issues.
• Conducts appropriate validation requirements, according to SOPs, for each task undertaken.
• Checks programming logs for cleanliness and correct processing of data. Inputs into Data Issues log and follows issues to appropriate resolution.
• Writes and maintains programming specifications datasets and programs assigned datasets to industry standards. Handles dataset derivations and assignment.
• Programs TLFs, maximizes programming efficiency with use of biostatistical tools, where applicable. Checks resulting output for format and co...