Senior statistical Programmer

Tasks

• Create ADaM datasets
• Create bioresearch monitoring reports
• Create clinical registry reporting files
• Create subject narratives
• Create tables, listings, and figures
• Define maintain clinical data analysis metadata
• Design develop and maintain SAS macros
• Develop validate electronic submission packages
• Implement generic SAS code for clinical trials
• Maintain data lineage and traceability from ADaM to SDTM
• Maintain specification documentation
• Perform QC of programmed output
• Preconfigure standards per data lifecycle plan

Perks/Benefits

• Professional development
• Remote work option
• Written and verbal communication

Skills/Tech-stack

ADaM | CDISC | Clinical Trial Data | Clinical trial | Controlled Terminology | Data Lineage | EMEA Submissions | Electronic submission | Electronic submission packages | FDA Submissions | ICH GCP | Python | QC | R | SAS | SDTM | Submission Packages | Trial data