SAS Programmer I

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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. We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Originally posted on Himalayas