RESPONSIBILITIES

• Participate in the development of study protocols including experimental designs, sample size determinations, coding specifications, data collection and entry rules to ensure all relevant data necessary for the studies are captured
• Develop statistical analysis plans including analysis files and report specifications
• Perform statistical analyses, interpret statistical results, and help prepare genetic study reports including summaries for FDA submissions
• Perform statistical and bioinformatics analyses of experimental data produced by MALDI-TOF MS, qPCR, Sequencing instruments
• Conduct data mining over internally produced and publicly available data sets
• Provide analysis information to management to aid in decision making on the development of new products
• Support creation of publication material from a statistical perspective

REQUIREMENTS

• PhD in Biostatistics/Computational Biology/Bioinformatics or related field
• 7+ years related experience in the statistical analysis of biological data
• Proficient in biological sequence analysis and analysis of next-generation sequencing data
• Strong knowledge of human genetics
• Proven track record of proficiency in data analysis and statistical learning
• Proficient with at least one of the following high level programming languages: R/S-PLUS (preferred), Matlab, SAS

• Experience in writing statistical plans, protocols, and reports
• Experience developing in a FDA QSR or ISO 13485 Design Control environment
• Programming experience in Java, Python or Perl and experience with databases and SQL highly desirable

LOCALE

COMPENSATION

HOW TO APPLY