viernes, 11 de octubre de 2013

SAS Programmer - CRO, UK

SAS Programmer - Global CRO, UK

My client is a global CRO and currently after a talented SAS Programmer to join them. This will be a full-time permanent position and will be either based from their offices or working remotely depending on your experience. The primary activity of the SAS Programmer will be to develop and review SAS programs and output for the management and reporting of clinical trial data. The individual in this role will have responsibilities including but not limited to the following:

About the Job:

* Participate in the Statistical Programming reviews
* Develop and review SAS programs and output as required
* Carry out electronic data transfer (both incoming and outgoing).
* Set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities.
* Review draft and final production runs for projects to ensure quality and consistency
About You:

* BSc in a computing, life science, mathematical or Statistical subject.
* Typically 2+ years' experience working as a Statistical Programmer in the clinical research industry
* An understanding of the fundamental principles of programming, program development and review
* Experience in the preparation of Programming Plans, study set-up and review of study specific documents

Ideally the right candidate will have knowledge of CDISC, SDTM and ADaM. For this role, you must be fully eligible to live and work in the UK.

If you are interested in this opportunity and wish to apply, feel free to get in touch. My contact details are below:

Sherry Bajwa - Biometric Consultant
sbajwa@i-pharmconsulting.com
+44(0)203 189 0465
More information: http://www.wileyjobnetwork.com/job/630066/sas-programmer-cro-uk/?TrackID=139218

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