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US: Scientist, Staff (Oncology)

Date: 11-May-2017
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Scientist, Staff (Oncology)

Be part of a team: initiating, developing, and validating IVD oncology kits for the liquid biopsy market Plan feasibility testing, protocol development, optimization, verification, validation, and launch Document research progress under a Quality Management System Communicate progress directly with colleagues and senior management Build and manage a small team of Research Associates Design effective experiments and work with statistics and bioinformatics team Perform basic data analysis (R, JMP, Excel) Successfully interact with various functional roles (including Marketing, Software, Engineers, Quality, Manufacturing & Project managers) within the organization to drive project to completion.

Ph.D. in oncology, molecular biology or closely a related field and at least 4 years of industry experience Excellent verbal and written communication skills, logical and analytical thinking, ability to multitask, work independently and on a team, and the ability to learn, troubleshoot, and problem solve Understanding and familiarity with CLSI guidance Product development for regulated markets (CE/IVD, FDA) is a huge plus Experience with nucleic acid technology relating to PCR, qPCR, multiplex PCR, and digital PCR Experience with next generation sequencing, target enrichment experience is a plus Very strong analytical and problem solving skills Adept with Excel, basic statistical analysis, programming (e.g. PERL, python) and databases experience (SQL) are a plus Skilled at writing clear plans, reports and SOPs, experience with Design Control a plus

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BioTech FYI Center
http://biotech.fyicenter.com/