Senior Statistical Programmer FSP

Tasks

• Create and review submission documents and eCRTs
• Create tables listings and figures for clinical trials
• Execute QC and validation programming
• Generate and validate SDTM and ADaM datasets and analysis files
• Generate complex ad hoc reports from raw data
• Perform clinical trial data manipulation analysis and reporting using SAS
• Perform define xml submissions
• Support efficacy analysis

Perks/Benefits

• Fully remote
• Training and development support

Skills/Tech-stack

ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Trial Data | Clinical trial | Data Validation | DefineXML | Efficacy analysis | Oncology | Quality Control | SAS | SDTM | Trial data