SAS Programmer for a large CRO!

An exciting opportunity has arisen with our client, a large CRO in their Germany site to join their quickly expanding Biostatistics and Programming department and take on a role of SAS Programmer! This challenging opportunity would be an ideal match for a professional within the industry who is fluent is fluent in both English and German.

As a SAS Programmer you will be reporting to the VP of global biostatistics and programming and will be highly responsible for biostatistical activities of clinical trial projects assigned under consideration of the regulatory requirements, ICH and other international guidelines. An essential part of this role will be generating, evaluating and validating SAS programmed as required within the evaluation process. This will also include plausibility checks and other quality control actions in biostatistical areas.

The ideal candidate will have a degree in medical sciences documentation or equivalent education. You will have a good knowledge of natural sciences and medical terminology and last but not least advanced knowledge of SAS software, including SAS Macro Language. This role will ideally fit to a professional with a good knowledge of coding of adverse events and a good experience in regulations and international guidelines.