Senior Statistical Programmer FSP
Tasks
- Communicate with cross functional teams for project specifications and status
- Create and review submission documents
- Create complex ad-hoc reports from raw data
- Generate and validate TLFs
- Generate validate SDTM ADaM datasets and analysis files
- Perform clinical trial data manipulation analysis reporting using SAS
- Perform production QC validation programming
- Submit using definexml and manage eCRTs
- Support efficacy analysis
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical data | Clinical data management | Clinical trials | Data Management | Efficacy analysis | QC | SAS | SDTM | Validation
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Roles
Related jobs
-
Senior Statistical Programmer FSP (SAS+R) EUR 63K-65KADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Trial DataFully remote | Training development supportSenior-level Full TimeSpain R2d ago
-
Senior Statistical Programmer FSP EUR 61K-73KADaM | CDISC | Clinical Trial Data | Clinical trial | Data QualityFully remote | Supportive work environment | Training and developmentSenior-level Full TimeSpain R3d ago