Senior Statistical Programmer FSP

Tasks

• Communicate with cross functional teams and clients for specifications and status
• Create and review submission documents and eCRTs
• Create complex ad-hoc reports from raw data
• Generate and validate ADaM datasets and analysis files
• Generate and validate SDTM datasets and analysis files
• Perform clinical trial data manipulation analysis and reporting
• Perform production QC validation programming
• Produce TLFs tables listings and figures
• Support efficacy analysis

Perks/Benefits

• Fully remote
• Training and development

Skills/Tech-stack

ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Reporting | Clinical data | Clinical data management | Data Management | Data Validation | Define-XML | Efficacy analysis | Quality Control | SAS | SDTM | TLF