Biostatistician

*Provide statistical input for protocol/CRF development (e.g., design; appropriate collection of observations in order to satisfy objectives; sample size estimation for the most efficient and practical design; patient randomization; accurate, logical, clear, concise and thorough evaluation of results section; effective CRF specifications to collect data specified in the protocol) and query checks.
*Write analysis plans for clinical trials including the most appropriate statistical methodology and data presentations.
*Write accurate, logical, clear, concise, thorough and objective statistical methods sections for integrated final reports.
*Review integrated draft reports ensuring the accuracy of the statistics.
*Perform statistical analysis for manuscripts
*Keep abreast of statistical developments
*Program and validate tables and derived listings as required.
*Understand and follow all statistical and statistical programming SOPs as well as any other relevant SOP.
*Communicate statistical concepts and results to non-statistical internal colleagues in a clear, concise, focused and articulate manner.
*Provide leadership to non-statistical colleagues with statistical issues
Essential Skills & Capabilities:

Minimum 2-4 years experience of statistics in a clinical trial environment.
Advanced degree (MSc or PhD) in statistics, biostatistics, mathematics, or related field, BSc qualifications will be considered with good relevant industry and statistical experience.
SAS programming skills are also required.

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