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• Being a Clinical Programmer performs data validation and develops algorithms for data management, typically using SAS programming language.
• Build SAS datasets from clinical database.
• Develop SAS macros, templates and utilities for data cleaning and reporting.
• Utilize SDTM guidelines to build datasets.
• Communicate with an internal team to create deliverables for pharmaceutical and biotechnology clients.
• Implement analyses specified in the protocol or the Statistical Analysis Plan (SAP) while working with the project statistician.
• Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.
• Write SAS programs to generate tables, listings, and figures and analysis datasets.
• Review CRF annotations and data specifications.
• Work in tandem with Biostatistics and Data Management member on various clinical projects.
• Identify and edit checks per the data validation plan or data management plan.
• Study management reports using SAS.