Offer summary
Qualifications:
University and master's degree in applied science, mathematics, or statistics, Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH), Good programming logic, SQL, and macro programming are preferred, Experience within clinical trials and/or Biostatistics, Proficient in spoken and written English.
Key responsabilities:
- Develop analysis data sets structure
- Program data sets, summaries, and support validations
- Prepare and review program documentation
- Produce TFL for clinical research projects
- Communicate with project teams regarding programming activities