to clinical programming. Review draft clinical reports, journal articles, slide presentations, and other documents to assure... or other relevant scientific fields; master's degree preferred. Minimum 6 years of experience in developing software for clinical...
Responsibilities: Develop and maintain SAS programs to import, clean, and validate clinical trial data. Use R... and analysis plans. Generate tables, listings, and figures (TLFs) using SAS and R. Create and QC statistical outputs and clinical...
/ Statistical SAS Programmer is responsible for providing programming support for clinical trials and contributing to the...***This is a remote position that can be worked from home anywhere in the United States*** The Senior SAS Programmer...
for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings..., and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. Interpret study...
for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings..., and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. Interpret study...
for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings..., and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. Interpret study...