Bioinformatics Data Scientist Position

3 weeks ago


San Francisco, California, United States Central Business Solutions Full time

Role Overview
As a Bioinformatics Data Scientist at Central Business Solutions, you will be part of a fast-growing field of Clinical Diagnostics developing algorithms for molecular diagnostics based on real-time PCR technologies. Our team has played a pivotal role in the COVID-19 pandemic with the Taq Path COVID-19 Combo Kit for testing SARS-CoV-2. We continue to innovate and provide new solutions for the pandemic and need your talent to help save lives.

Key Responsibilities
• Organize and data mine clinical data to assess the performance of clinical tests
• Work closely with scientists and engineers with data analysis & experimental design
• Develop software and analysis pipelines for data mining large datasets and auto generation of reports
• Develop classification algorithms and model data
• Evaluate algorithms needed for filtering, clustering and qualification of data and perform root cause analysis
• Collaborate and communicate with various teams and business units

Requirements
• Bachelor's degree in Molecular Biology, Biology, Chemistry, Applied Mathematics, Physics, Electrical Engineering, Computational Biology, Biostatistics, Bioinformatics, Computer Science or related discipline; postgraduate degree (Master's, PhD) is highly preferred
• 3+ years of product development experience (biotechnology industry preferred)
• Strong hands-on data analysis, modeling, and classifiers experience
• Data structures and common methods in data transformation
• Pattern recognition and predictive modeling skills
• Excellent programming skills in C++, Java and Python
• Experience utilizing Matlab, JMP, R, PowerBI or SPSS
• Experience working in regulated/validated environment is a major plus
• Knowledge, Skills, Abilities Understanding of clinical trial design and evaluation
• Knowledge in Molecular Biology and Clinical Diagnostics
• Strong understanding of qPCR and amplification curve data
• Prior experience with US-FDA 510k product development/submission, 21 CFR Part 11, and ISO 13485 is highly preferred
• Ability to present and communicate analytical and clinical study analysis results to non-experts
• Ability to work independently and in a team environment



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