(Senior) Statistical Programmer

As a Statistical Programmer you will be responsible for reporting (clinical) trials. Your activities will consist of the analysis and reporting of clinical and pre-clinical trials using the SAS programming language. Our clients are leading companies in the life sciences industry in areas such as pharmaceutics, nutrition, and devices. At OCS Consulting, we work in a hybrid setup, meaning you can work from home, from our office, or occasionally from a client's site. We value flexibility, collaboration, and a healthy work-life balance.

You have sound knowledge of SAS Base and SAS Macro. You know what it means to work in a regulated environment and are aware of the importance of quality. You are able to deliver within the expected timeframe. Furthermore you know how to adapt to your working environment: formal when required, informal when possible. In addition, you:

• have experience with CDISC - bring at least three to five years of experience with SAS Base and SAS Macro - are at least SAS Base certified, or have the willingness to obtain the certificate - are professionally proficient in the English language, both spoken and written - have an enthusiastic and motivated personality - have an independent and pro-active attitude.

Why Join OCS Consulting? OCS Consulting has a long-standing partnership with SAS Institute and is a trusted partner for the Life Science industry. We have been named SAS Solution Provider and Partner of the Year multiple times. This not only shows our strong connection to SAS but also the excellence of our consulting team and the quality of our services, which gives you a head start. We valu...