Senior Statistical Programmer FSP

Tasks

• Communicate with cross-functional teams
• Create and review submission documents
• Create and validate TLFs
• Generate and validate ADaM datasets
• Generate and validate SDTM datasets
• Generate complex ad-hoc reports
• Perform SAS programming for clinical trial data manipulation
• Perform production QC and validation programming
• Prepare eCRTs
• Support efficacy analysis

Perks/Benefits

• Fully remote
• Global team collaboration
• Training and development

Skills/Tech-stack

ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical trials | Data Analysis | Data Manipulation | Data reporting | DefineXML | Development Life Cycle | Drug development | Drug development life cycle | Efficacy analysis | Oncology | QC validation | SAS | SDTM