Senior Statistical Programmer FSP
Tasks
- Apply efficacy analysis methods
- Communicate with cross functional teams for project specifications and status
- Create and review submission documents and eCRFs
- Create complex ad hoc reports using raw data
- Generate and validate SDTM and ADaM datasets and analysis files
- Perform SAS data manipulation analysis and reporting of clinical trial data
- Produce and perform QC validation programming
- Serve as study lead when needed
Perks/Benefits
Skills/Tech-stack
ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Data Interchange Standards | Clinical Data Interchange Standards Consortium | Clinical data | Clinical trials | Data Validation | Define-XML | ECRF | Efficacy analysis | Pharmaceutical Development | Quality Control | SAS | SDTM
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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