Job Description
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.
Please note your CV should be submitted in English
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 degree in applied science, mathematics, statistics or similar
Strong knowledge of and experience with SAS software
Good knowledge of programming logic, SQL and macro programming is preferred
Full proficiency in English, spoken and written
Previous experience working with clinical trials
Good analytical skills
Proficiency in standard MS Office applications
Excellent communication and interpersonal skills 
