You will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.
You will:
- Develop analysis data sets structure
- Develop program requirements and specifications
- Be involved in SAS programming of ADS and Tables Listings and Figures
- Support SAS program validations
- Prepare and review program documentation
- Produce TFL
- Communicate with project teams and company departments with regard to statistical programming of clinical research projects
Qualifications :
- University and masters degree in applied science mathematics statistics or the like
- Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system
- Good knowledge of programming logic SQL and macro programming is preferred
- Proficient in English spoken and written
- Experience within clinical trials and/or Biostatistics
- Good analytical skills
- Proficiency in standard MS Office applications
- Excellent communication and interpersonal skills
Please submit your CV in English
Remote Work :
Yes
Employment Type :
Fulltime