Senior Statistical Programmer FSP

Tasks

• Analyze safety and efficacy data
• Communicate with cross-functional teams
• Create ad-hoc reports
• Generate and validate datasets TLFs reports and submission documents
• Lead projects when required
• Manipulate clinical trial data
• Perform programming QC and validation
• Support phases I-IV clinical trials

Perks/Benefits

• Collaboration environment
• Flexible remote work
• Training and development

Skills/Tech-stack

CDISC ADaM | CDISC SDTM | Clinical Trial Data | Clinical trial | Data Analysis | Data Management | Data Manipulation | Data reporting | Efficacy analysis | QC validation | Reporting | SAS | Trial data