Designs, plans, and executes biostatistical components of clinical trials. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.
•Serves as the lead biostatistician on project teams for simple to moderate clinical studies.
•Develops statistical analysis plans and reporting specifications for simple to moderate clinical studies.
•Performs statistical analyses and interprets results from simple to moderate clinical studies.
•Participates in the development and review of CRFs, edit specifications, and critical variable lists.
•Performs lead review of TFLs and derived datasets for clinical studies.
•Contributes to clinical study protocols and clinical study reports.
•Reviews simple to moderate randomization specifications and dummy randomizations.
•Participates in bid defense meetings.
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