Senior Manager, Statistics (Oncology)

Key Responsibilities

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.

Education & Experience

• PhD in Statistics, Biostatistics, Mathematics, or a highly related field & 2 years of work experience performing statistical data analyses. Must have 2 years of each of the following:
• performing data analyses & simulations which support new drug application &/or post market medical studies;
• identifying data or analytical issues, & assisting with providing solutions;
• conducting scientific research in clinical trial study designs, inferential statistics, causal inference; &
• using SAS &/or R statistical software for statistical analyses, statistical computation & simulations
• Alternatively, Master's in Statistics, Biostatistics, Mathematics, or a highly related field with at least 5 years of work experience performing statistical data analyses. 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.

Pay

$169,950 - $236,500 per year.