Manager, Statistics - South San Francisco, United States - AbbVie

AbbVie

Verified Company

South San Francisco, United States

2 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Company Description

Job Description Key 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 highquality outputs according to agreedupon 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.

Qualifications
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 in the following:

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.

Salary Range:
$160, $181,500.00 per year
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Additional Information

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

This job is eligible to participate in our short-term and long-term incentive programs.