Please submit your CV in English.
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
- University and Master's 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 is desirable
- 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
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.