Provide expertise to design, analysis & reporting of clinical trials or other scientific research studies. Implement sound statistical methodology in scientific investigations. Identify & anticipate issues arising in the study design. Conduct & propose scientifically sound approaches. Assess needs for potential development of novel statistical methodology. Independently develop protocols and/or statistical analysis plans with details for programming implementation. Develop strategy for data presentation & inference. Ensure that study results & conclusions are scientifically sound, clearly presented, & consistent with statistical analyses provided. Work collaboratively with multifunction teams.
Must possess PhD in Statistics, Biostatistics, Mathematics, or a highly related field & 2 years of work experience performing statistical data analyses. Of the experience required, must have 2 years of each of the following: (i) performing data analyses & simulations which support new drug application &/or post market medical studies; (ii) identifying data or analytical issues, & assisting with providing solutions; (iii) conducting scientific research in clinical trial study designs, inferential statistics, causal inference; & (iv) using SAS &/or R statistical software for statistical analyses, statistical computation & simulations. Alternatively, would accept a Master's in Statistics, Biostatistics, Mathematics, or a highly related field with at least 5 years of work experience performing statistical data analyses. Of the experience required, must have 5 years of experience with (i) through (iv). Of experience required with either combination, must have 2 years performing statistical data analyses in the pharmaceutical industry. Work experience may be gained concurrently. Employer will accept any suitable combination of education, training, or experience.
Apply online at https://careers.abbvie.com/en or send resume to [email protected]. Refer to Posting REF49826Q.
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