C. R. Bard, Inc.


Posted Date 2 months ago(1/15/2018 10:09 PM)
Industry / Category
Quality Systems Engineer
Job ID
Career Level
Bard Medical


The Statistician position is located in Covington, GA at Bard Medical a division of BD.

Summary of Position with General Responsibilities

The Statistician is responsible for timely and high quality data review and query management of data supporting Bard Medical.  The Statistician develops and maintains key data management deliverables used to collect, review, monitor, and ensure the integrity of medical devices.



Essential Job Functions

  • Use statistical expertise to prepare both internal and external reports and presentations with the aim to improve the quality of internal decision making
  • Bring innovative statistical thinking and methods to maximize the value of aggregate data in support of medical device development strategies
  • Understand business needs and deliver targeted analytics to cross-functional franchise teams and other key stakeholders to equip staff with compelling information and evidence for design sessions
  • Use advanced statistical and predictive modeling techniques to build, maintain, and improve multiple real-time decision capability
  • Ensure statistical rigor and good scientific practices are followed, excellent statistical methods utilized, and documented in protocols, analysis plans and reports
  • Anticipate and identify opportunities for Analytics to support novel study designs and targeted identification of operational risks
  • Identify available and relevant data, including internal and external data sources, and leverage new data collection processes
  • Develop statistical tools to aid scientists in standardized analyses.
  • Developing innovative and effective approaches to solve analytics problems and communicates results and methodologies
  • Developing innovative and fit-for-purpose analytical strategies


Education and/or Experience

  • Masters in Statistics, Mathematics, Biostatistics, Machine Learning or related quantitative field with a minimum of three (3) years of FDA regulated industry experience in quality engineering, operations research, market research, or applied statistics or PhD with at least 2 years’ experience with data collection/statistics for clinical trials 
  • Technical skills/knowledge in one or more of the following:  SAS and/or SQL programming experience , multivariate analysis, regression analysis and forecasting, sampling, data modeling, R programming, machine learning, SPSS
  • Computer literacy in MS Word, Excel, PowerPoint etc. 
  • Trackwise or similar system experience
  • Experience working with medical device failures/claims-level data
  • Experience analyzing very large amounts of data
  • Excellent communication (written and verbal), attention to detail and interpersonal skills


Physical Demands

Employee may be required to sit, bend, stoop, use keyboard, see, talk and hear.  May occasionally lift objects up to 25 lbs.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Work Environment

Normal office environment - noise level is quiet to moderate - frequent travel is required - when traveling to clinical sites or hospitals, work environment will be specific to the area under evaluation.





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