SAS Programmer I

Job Description

Please submit your CV in English.
You willcontribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets andsummaries.

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
• Prepareand review program documentation
• Produce TFL
• Communicatewith project teams and company departments with regard to statistical programming of clinical research projects

Qualifications

• University and Master's degree in Statistics or Biostatistics
• 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 inEnglish, spoken and written
• Experience within clinical trials and/or Biostatistics
• Good analytical skills
• Proficiency in standard MS Office applications
• Excellent communication and interpersonal skills

Additional Information

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.