Clinical SAS Programmer

CHDR is looking for a Clinical SAS Programmer for 27 – 40 hours a week

April 2017

Key Tasks and responsibilities:

  • Developing SAS programs to create interim and final safety analysis reports, transfer files and transform received data to the requested format;
  • Validating SAS programs and perform output validations;
  • Reviewing study protocols;
  • Defining study databases including edit checks (at CHDR we use the integrated clinical data management and EDC system Promasys®);
  • Reviewing and writing Data Transfer Plans
  • Mapping study data to SDTM, including the define-XML;
  • Validating SDTM domains and define-XML;
  • Writing SOPS.


  • At least 3 years of experience in SAS programming within the pharmaceutical industry/CRO;
  • Experienced in creating Tables, Listings and Figures;
  • Expertise in defining/building study databases (eCRF) and creating edit checks;
  • Expertise in CDISC (Controlled Terminology, SDTM, ADaM, define-XML, Annotated CRF) is a pre;
  • Knowledge and understanding of the ICH Guidelines, FDA Industry Guidelines and GCP principles;
  • Good English written and oral communication skills;
  • Feeling comfortable in an environment where working with stressful periods is common.


  • Accurate
  • Team player
  • Result minded
  • Able to work independently and within timelines;
  • Good communication skills;
  • Quality awareness.

If you are interested in this position, please send an application with a motivation letter and cv to or by mail to M.ten Kate, HR Manager, CHDR Zernikedreef 8, 2333 CL Leiden. If you want some more information, please don’t hesitate to call Alexa Tibboel 071-5246455 or Ria Kroon 071-5246498;