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Dear Allstat,

My client is looking for a SAS programmer to work no more then a few days  a week starting from July on a contract basis of 6 months. This position is based in Edinburgh and the rate is negotiable. 

	Break down of role :- 	90% Managing clinical study data
	 	 		5% Deliver Global R&D and ISMO Clinical Plans
				5% Delivery of Quality, Compliance & Governance Standards

*	Responsible for performing a range of SAS programming duties including the development of programs to validate study data, the listing of study data, the performance of statistical analyses, the production of report and manuscript appendices and tables 
*	Plan, conduct and complete assigned project work, providing timely progress reports as required
*	Production of specifications, transfer file formats and processes for transmission and loading of data files from external/third party vendors
*	Develop eCRF modules, data checks and WBDC study database set up
*	Promote and use standard TA/Project module Package standards (e.g. data standards, loading and extract specs, edit checks, eCRF tables)
*	Develop expertise in e-clinical based studies.
*	Provide SAS and technical expertise and advice as required to TA/ Study Delivery Teams, ISMO, Global R&D, and CRR-EU as required
*	Comply with a culture of continued inspection readiness 
*	Comply with internal AstraZeneca clinical and marketing company governance guidelines
*	Maintain knowledge of relevant clinical processes and SOPs to ensure appropriate compliance to ICH GCP/ABPI code of practice

	If you are interested in this role please send a CV to :- [log in to unmask]

	Kind regards


Kien-Sen Lee
Resourcer ~ Biostatistics Division
James Harvard Pharmaceutical Ltd

T. 020 7922 7126   F. 020 7922 7101
E: [log in to unmask]    
W: www.jamesharvardpharma.com

25 - 27 Wootton Street : Waterloo : London : SE1 8TG

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