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Posted: Tuesday, April 4, 2017 12:34 AM

Boston Scientific Neuromodulation is currently seeking an exceptional Principal Biostatistician to join our winning team in Valencia, CA.

Why join Boston Scientific Neuromodulation in California?
We integrate all global operations at our worldwide headquarters in Valencia, California, close to Los Angeles, close to the beach, close to the mountains, close to the desert. All the advantages of Southern California and more affordable than many other areas nearby. Looking for onsite amenities? Check out our on:campus Bistro, Credit Union, private gym, and Toastmasters club. Take advantage of the 360 days of sunshine a year on our basketball and volleyball courts. Join our softball and soccer teams. We even have cricket and dragon boat racing teams We also offer numerous volunteer activities and events in the wonderful communities of Valencia and Santa Clarita. If you like to work hard and play hard, youll fit right in. And youll be well rewarded. Our salaries are competitive. Our benefits package is generous. And our 401K program? Forbes ranks it one of the top 10 in the country

What makes Boston Scientific Neuromodulation so special?
Weve seen the difference that neuromodulation technologies, such as spinal cord stimulation and deep brain stimulation, can make. These breakthrough platforms have helped more than 400,000 people worldwide over the past four decades. But there is still enormous potential to help even more people. As a worldwide leader in neurological devices, we strive to improve every life we touch through our dedication to innovation, our commitment to people, and our passion for performance.


Responsible for biostatistical activities in support of clinical trials including: providing innovative statistical solutions for scientific decision making, preparing statistical analysis plans, writing statistical section of clinical study protocols, generating data tables, patient data listings and report using SAS, performing analysis of clinical trial data and contributing to the interpretation of clinical trial data.

Key Responsibilities

: Work with Clinical Science and Clinical Operations staff to develop scientifically sound clinical study designs and write the statistical section of clinical research protocols
: Perform sample size calculations and simulations
: Provide input to database requirements and SAS data set specifications
: With the programmer, generate statistical summary tables, patient data listings and reports using SAS
: Prepare statistical analysis plans.
: Perform statistical program validation and handle complex study programming issues
: Contribute to the interpretation of clinical trial data and lead statistical methods and results section of the clinical study reports and scientific communications (presentations/manuscripts).

Basic Qualifications

: M.S. in Statistics, Biostatistics or related field.
: 7+ years of experience in the design and analysis of clinical studies or 4+ years with a Ph.D. degree.

Preferred Qualifications

: Ph.D. in Statistics or Biostatistics
: Experience applying adaptive design and Bayesian methods to clinical trials
: Experience in medical device, biotechnology or pharmaceutical industries
: Proficient programming skills in SAS, R or SPlus; experience using SQL and EDC highly desirable
: Knowledge of clinical trial methods and execution in a regulated environment
: Strong interpersonal and customer:focused skills; exceptional ability to drive results through strong collaborating and influencing skills across all business segments and geographies
: Demonstration or evidence of leadership competencies
: Demonstration of strong oral and written communication skills, including experience presenting clinical trial results and statistical methods
: Working knowledge and understan


• Location: San Fernando Valley

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