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.

Requirements:

  • 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.

Competencies:

  • 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 pz@chdr.nl 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;


Apply