Senior Statistical Programmer FSP
Tasks
- Coordinate with cross functional teams for project specifications
- Create TLF tables listings figures
- Create complex ad-hoc reports
- Create review submission documents
- Generate validate ADaM datasets
- Generate/validate SDTM datasets
- Perform QC validation programming
- Perform SAS programming for clinical trial data
- Provide study lead duties when needed
- Support eCRT development
- Support efficacy analysis
Perks/Benefits
Skills/Tech-stack
Ad Hoc Reporting | Ad-Hoc | CDISC ADaM | CDISC SDTM | Clinical Trial Data | Clinical trial | Data Manipulation | Data Validation | Data reporting | Define.xml | Efficacy analysis | QC validation | Quality Control | SAS | Submission documentation | Trial data
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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