Senior Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35)
Tasks
- Collaborate with biostatistics data management and clinical teams
- Create datasets, tables, listings, and figures
- Develop validate and maintain SAS programs for clinical study analysis and reporting
- Ensure programming deliverables meet quality standards
- Generate and validate SDTM and ADaM
- Generate and validate TLFs
- Participate in study planning review specifications and support submission activities
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical Practice | Clinical programming | Clinical trial | Clinical trial process | Data Validation | Good Clinical Practice | ICH GCP | SAS | SDTM | Stakeholder management | TLF | Trial process
Education
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