Senior/Principal Statistical Programmer SAS + R (Remote)

Tasks

• Author SOPs and work instructions
• Conduct exploratory analyses
• Contribute to programming tool standards
• Create CRFs
• Create define xml files
• Define edit check specifications
• Develop SAS programs
• Develop and validate SAS and R programs
• Develop data validation plans
• Follow good clinical practice guidelines
• Generate ADaM specifications
• Generate SDTM specifications
• Maintain SAS and R programs
• Oversee CRO programming deliverables
• Prepare DSUR
• Produce clinical tables listings and graphs
• Review data transfer specifications
• Support clinical study reports
• Support publications
• Support regulatory submissions

Perks/Benefits

• Career development
• Remote work
• Support
• Training

Skills/Tech-stack

ADaM | CDISC | CRF | Clinical Practice | Clinical programming | Clinical trials | Data Validation | Data transfer | Define.xml | Edit checks | Electronic submissions | FDA Regulations | Git | Good Clinical Practice | ICH Guidelines | R | SAS | SAS Macros | SDTM | Unix/Linux