> Dear Allstat,
>
>
> I have 3 brand new contract Stats roles to be based in the South East to start in Feb/March. The initial contract is for 12 months and may go longer. Ideally the candidates should have 5+ years background in stats and the writing of Statistical Analysis Plans (SAPs) within a pharma environment.
>
> You will be required to Provide statistical input to new protocols: draft the statistical sections. Review the sections on study design and description of clinical endpoints.
> For ongoing studies, advise on data collection: this includes review of the proposed CRF.
>
> Prepare the data analysis for the clinical study report: review protocol deviations/violations, confirm the validity of the original statistical analysis plan, program and conduct the original exploratory efficacy analysis, review the formal safety and efficacy tables produced by reporting statisticians.
>
> If this sounds like the kind of role you would be interested in hearing more about please contact me for more details.
>
> Mark O> '> Brien
> Consultant ~ Clinical & Biometrics
> James Harvard Pharmaceutical Ltd
>
> T. 020 7922 7106 M. 07921 176225 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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