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Dear Allstat I am handling an urgent requirement with a clinical trials company in the London area for a Principal Biostatistician. The role can either be permanent or offered on a 12 month contract basis. My client can only consider those with a 4 week notice period or less. In this role, you will be providing statistical input, mainly in the phase I area, for protocol/CRF development (e.g., trial design; sample size calculations for the most effective design, patient randomisation, accurate, logical, clear, concise and thorough evaluation of results section, effective CRF specifications to collect data specified in the protocol. You will be required to ensure analysis plans include the most appropriate statistical methodology and data presentations, review and co-author clinical trial reports ensuring the accuracy of the statistical interpretation, keep abreast of statistical developments, understand and follow all Global Biostatistics SOPs & communicate statistical concepts and results to non-statistical internal and external colleagues. The ideal candidate will posses an MSc or PhD in Statistics with significant experience within either a CRO or pharmaceutical environment. You must be eligible to work in the UK and posses excellent written and spoken English. To apply, please send your CV to [log in to unmask] or for further information please call +44(0)207 562 1792 Thank you and best wishes Helena Helena Newman-Mitchell Biometrics Lead Direct: +44 (0) 207 562 1792 Fax: +44 (0) 207 562 1799 Mobile: +44 (0) 782 536 2548 Email: [log in to unmask] Website: www.srgclinical.com <http://www.srgclinical.com/> <blocked::http://www.srgclinical.com/about/ICR2009.aspx> You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.