Delivering on the promise of medical innovation begins at Boston Scientific.
By delivering innovative products that help clinicians improve the lives of patients every single day, Boston Scientific makes a profound impact on the quality of medical care around the world. As we continue to transform the field of medical technology, we seek dedicated individuals who possess the integrity and creative spirit needed to thrive in an innovative company. Join a global organization that is fueled by the diversity and talent of its entire workforce.
Biostatistician
Description
General Summary:
This position is responsible for biostatistical activities in support of clinical trials including: generating data tables, patient data listings and reports using SAS; preparing statistical analysis plans; contributing to the statistical section of clinical trial protocols; reviewing analysis of clinical trial data.
Duties and Responsibilities:
Under direct supervision performs the following duties:
• Generates statistical summary tables, patient data listings and reports using SAS.
• Performs quality control check of SAS programs.
• Handles basic SAS programming issues as well as all other study programming issues.
• Assists with UAT of SAS dataset transfer files.
• Works with the Biostatistics Manager and Clinical Sciences staff to develop scientifically sound clinical study designs and contributes to the statistical section of clinical research protocols.
• Contributes to or prepares statistical analysis plans under the direction of the Biostatistics Manager.
• Prepares template and performs programming for periodic progress reports for assigned clinical programs.
• Compiles clinical data and relevant background material, and presents these results to the Biostatistics Manager for review.
Minimum Education & Experience:
• Master's level degree in biostatistics, statistics, or public health; Bachelor's level degree will be considered.
• At least 1 year of experience in SAS programming; preferably 1 year in medical device or pharmaceutical clinical trials.
• Demonstrated computer expertise in SAS programming and word processing; experience using SQL and EDC highly desirable.
• Familiarity with clinical trial design and analysis issues.
Working Conditions:
General office environment, minimal travel.
