Dear Allstat,
I have 2 brand new contract Stats role to be based in Kent to start in November. The initial contract is for 3 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.
Kind regards, Mark
Mark O'Brien
James Harvard Pharmaceutical Ltd
T. 020 7269 5006 M. 07921 176225 F. 020 7269 5009
e: [log in to unmask] w: www.jamesharvard.com <http://www.jamesharvard.com/>
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