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Modeling and Simulation - Principal Statistician

Posted on Apr 5, 2021 by Amgen

Newbury Park, CA 91319
Research
Immediate Start
Annual Salary
Full-Time


Let's do this. Let's change the world. In this vital role you will be accountable for the development and execution of the simulation plan based on design options and simulation specifications provided by DSI, SDD and study teams; and deliver simulation reports under the guidance from DSI.


Participates in discussion sessions of EGP development and study design to ensure understanding of the clinical trial design options and collect design inputs from DSI, SDD and study team
Works with DSI to develop and finalize simulation plan with detailed specifications and operating characteristics that enable the evaluation and selection of the optimal design options
Executes simulation plan and summarizes results in outputs in presentation ready visualization
Works with DSI to evaluate design options and form design recommendations and finalize simulation report
Participates in sessions to present simulation results and recommendations to the product/study team
Leads the development of modeling and simulation tools
WIN
WHAT WE EXPECT OF YOU


We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborator with these qualifications.


BASIC QUALIFICATIONS
Doctorate degree and 2 years of Statistical Modeling and Simulation experience Or
Master's degree and 6 years of Statistical Modeling and Simulation experience Or
Bachelor's degree and 8 years of Statistical Modeling and Simulation experience Or
Associate's degree and 10 years of Statistical Modeling and Simulation experience Or
High school diploma/GED and 12 years of Statistical Modeling and Simulation experience
PREFERRED QUALIFICATIONS
Master's degree in Statistics/Biostatistics or related subject with high statistical content with 6 years of post-graduate statistical experience in the biopharmaceutical industry in clinical trial design, execution, analysis and reporting; or
Doctorate in Statistics/Biostatistics with 4 years of post-graduate statistical experience in the pharmaceutical industry or medical research
Experience in designing, analyzing and reporting of clinical trials within Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia
Excellent computing, modeling and simulation skills using R, SAS, WinBugs, FACTS, etc.
Proactive and efficient in learning emerging adaptive designs and building simulation tools and interactive visualizations for wide use and applications




Reference: 1152695042

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