Senior Statistical Programmer FSP

Tasks

• Analyze clinical trial data
• Build QC validation programs
• Communicate with cross-functional teams
• Create TLF tables listings figures
• Create submission documents
• Generate ADaM datasets
• Generate SDTM datasets
• Generate ad hoc reports
• Perform SAS data manipulation
• Perform efficacy analysis
• Respond to project specifications status issues inquiries
• Review definexml and eCRTs
• Validate SDTM and ADaM data

Perks/Benefits

• Fully remote
• Supportive work environment
• Training and development

Skills/Tech-stack

ADaM | CDISC | Clinical Trial Data | Clinical trial | Data Quality | Data Validation | Data quality control | Efficacy analysis | Immunology | Oncology | Quality Control | Respiratory Studies | SAS | SDTM | Trial data