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Position: Senior Biostatistician
, Antwerpen , Frankfurt , Berlin , Irene , London , Belville , Reading , Brussels , Bloemfontein , Belgium , Germany , Netherlands , United Kingdom South Africa
Duties: Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports.Provide training, guidance and mentorship to lower level and new staff
Requirements: PhD in Biostatistics or related field and 3yearrelevant experience/Master's degree in Biostatistics or related field and 6 years relevant experience/Bachelor's degree in Biostatistics or related field and 8 years relevant experience; or equivalent combination of education, training and experience; In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trials; Strong individual initiative; Strong organizing skills; Strong working knowledge of SAS computing package
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