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Overview

Company

Original Job Post

BioSpace · 2 days ago

Manager, Statistics

South San Francisco, CA

Full-time

Onsite

Senior Level

$160K/yr - $182K/yr

2+ years exp

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Comp. & Benefits

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Responsibilities

Develop statistical methodology for protocols with details for programming implementation.

Provide expertise for design, analysis & reporting of clinical trials & other scientific research studies. Implement statistical methodology in scientific investigations.

Identify scientifically appropriate data collection instruments.

Identify & report data issues or violations of study assumptions.

Provide programming specifications for derived variables & analysis datasets.

Perform statistical computations & simulations as per the analysis plan to ensure the delivery of high-quality outputs according to agreed-upon timelines.

Identify & anticipate issues arising in the study design as well as conduct & propose scientifically sound approaches.

Evaluate appropriateness of available software for planned analyses & assess needs for potential development of novel statistical methodology.

Utilize experience with Statistical Analysis System (SAS) software, R software, & familiarity with software tools for designing statistically optimized clinical trials.

Develop strategy for data presentation & inference.

Collaborate in publication of scientific research.

Ensure accuracy and internal consistency of reports & publications, including tables, listings, & figures.

Ensure that study results & conclusions are scientifically sound, clearly presented, & consistent with statistical analyses provided.

Work collaboratively with multifunctional teams & provide responses to questions, & pursue analyses suggested by data.

Support communications between assigned product teams & functional management.

Qualification

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Statistical Analysis System (SAS)R softwareClinical trials designStatistical computationsStatistical simulations

Required

Must possess a PhD degree or foreign academic equivalent in Biostatistics, Statistics, or a highly related statistical field of study with at least 2 years of experience

Providing expertise for design, analysis & reporting of clinical trials & other scientific research studies

Performing statistical computations & simulations

Experience with Statistical Analysis System (SAS) software, R software, and familiarity with software tools for designing statistically optimized clinical trials