Sr Field Genomics Support Scientist
IlluminaAbout the role
In your role as Senior Field Genomics Support Scientist, you will have the opportunity to work with key opinion leaders throughout the United States and Canada to help them implement and innovate with our industry leading genomic analysis platforms including Emedgene and Illumina Connected Insights. You will develop deep scientific and technical knowledge of the platform and its capabilities and use it to help our customers quickly scale their ability to interpret genomic data and cultivate successful customer relationships.
Your feedback and expertise will also be critical to driving innovation in the platform through frequent work with our product development team. You will have the opportunity to advocate for your customers��� needs and to participate in early access and feedback for new versions. You will also work alongside an award-winning team skilled at partnering with customers to improve all aspects of our customers informatics environment from wet lab to secondary and tertiary analysis.
If you’re passionate about the future of genomics, enjoy a multi-disciplinary, fast-paced and innovative environment, and have great communication, project management, and technical skills, this is the role for you!
Responsibilities:
Develop a deep scientific and technical knowledge of the Illumina’s genomic analysis products with a focus on tertiary products
Connect customer requirements with platform functionality to streamline analysis workflows and ensure customer success
Use genetics and platform knowledge to consult with customers and optimally implement analysis SOPs to customer requirements
Work closely with the technical support and development teams to troubleshoot and solve challenging genomic analysis problems
Consult as a commercial subject matter expert for Illumina software solutions
Participate in productization discussions for new platform features. Test new platform features and gather feedbackfrom current customers.
Requirements:
Typically requires a minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree; or a PhD without experience; or equivalent work experience.
Experience in genomic variant interpretation required, including applying guidelines set out by ACMG and ClinGen for SNVs and CNVs. This experience should include working with population frequency databases (gnomAD, DGV, etc.), classification databases (ClinVar, ClinGen, MitoMap, etc.) in silico prediction models (REVEL, spliceAI, CADD, etc.) and disease databases (OMIM, MONDO, Orphanet, etc.).
Working understanding of sequencing data analysis including common alignment and variant calling tools and file formats required.
Experience in writing variant interpretations and genetic test reports preferred.
Prior experience supporting customers especially in a highly scientific / technical field preferred
Excellent troubleshooting, communication, organizational and interpersonal skills highly valued
MS or PhD in a Life Science degree (Genetics, Molecular Biology, Computational Biology) or equivalent genomic research or clinical background preferred
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