Senior Statistical Programmer FSP (SAS+R)

Tasks

• Analyze clinical trial data
• Create ADaM datasets
• Create Define xml
• Create SDTM datasets
• Create submission documents
• Generate ad-hoc reports from raw data
• Generate clinical trial reports
• Manipulate clinical trial data
• Perform QC validation programming
• Perform efficacy analysis
• Produce TLFs
• Produce figures
• Produce listings
• Respond to project specifications status issues
• Review submission documents
• Validate ADaM datasets
• Validate SDTM datasets

Perks/Benefits

• Development
• Fully remote
• Support
• Training

Skills/Tech-stack

CDISC ADaM | CDISC SDTM | Clinical Trial Data | Clinical data | Clinical data standards | Clinical programming | Clinical trial | Data Standards | Data Validation | Define-XML | Efficacy analysis | QC validation | R | SAS | TLF | Trial data