Senior Biostatistician
BioPhase Solutions - San Diego, CA

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BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Senior Biostatistician to work for a leading San Diego biotechnology company.
Senior Biostatistician

Reporting to the Director of Bioinformatics, the Senior Biostatistician is responsible for developing algorithms and performing data mining and statistical analyses for molecular biology experiments. The ideal candidate must be able to work in a collaborative research environment and provide evidence of relevant research expertise in the form of technical publications, presentations, software, and/or knowledge of applications.

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

Performs 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 with Laboratory Developed Tests (LDT) and/or In-vitro Diagnostics (IVD) highly desirable

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

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