Clinical Biostatistician - Vista, CA - KatalystHLS.com Manage Bio statistics staff and statistical programmers as appropriate, including but not limited to resource planning, recruitment, performance evaluations, and training. Coordinate and oversee statistical analyses and programming activities on clinical trials. Facilitate interaction and communication between Bio statistics and other members of the project teams to which s/he is assigned (Clinical, Data Entry, Medical Writing, Data Management, Safety, Project Management, etc.). Represent the Sponsor, when required, in discussions and meetings with the FDA. Develop study-specific Statistical Analysis Plans based upon the protocol, clinical monitoring plan and Case Report Forms (CRFs) to ensure that the data collected during clinical trials are analyzed using appropriate analyses and are reported to a level appropriate to meet regulatory requirements. Manage the implementation of all Statistical Analysis Plans with the statistical
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