Senior Statistical Programmer FSP

Tasks

• Communicate with cross-functional teams
• Create TLF tables listings figures
• Create review eCRTs
• Create review submission documents
• Generate SDTM ADaM datasets
• Generate ad hoc clinical reports
• Perform SAS QC validation programming
• Perform clinical trial data manipulation
• Respond to project specifications status issues
• Support efficacy analysis
• Validate SDTM ADaM datasets

Perks/Benefits

• Fully remote
• Support
• Training and development

Skills/Tech-stack

Ad Hoc Reporting | Ad-Hoc | CDISC ADaM | CDISC SDTM | Clinical data | Clinical trials | Data Analysis | Data Manipulation | Define-XML | Efficacy analysis | QC validation | SAS | TLF