
Clinical Variant Interpretation Scientist (Remote)
MyOme
Full time
Other
United States
Hiring from: United States
About MyOme
MyOme’s mission is to provide clinically actionable genetic information to patients throughout their lives. We combine clinical-grade whole genome sequencing, advanced methods for genome interpretation, and seamless digital tools for doctors and patients to order and access results. Our team is composed of seasoned entrepreneurs, scientists, and operators, and we're backed by top-tier investors.
Job Description
MyOme is seeking an experienced and motivated Clinical Variant Interpretation Scientist to lead variant interpretation efforts. In this role you will help develop internal documentation including interpretation SOPs and reporting policies in collaboration with our clinical team.
Responsibilities
Join us if you:
MyOme’s mission is to provide clinically actionable genetic information to patients throughout their lives. We combine clinical-grade whole genome sequencing, advanced methods for genome interpretation, and seamless digital tools for doctors and patients to order and access results. Our team is composed of seasoned entrepreneurs, scientists, and operators, and we're backed by top-tier investors.
Job Description
MyOme is seeking an experienced and motivated Clinical Variant Interpretation Scientist to lead variant interpretation efforts. In this role you will help develop internal documentation including interpretation SOPs and reporting policies in collaboration with our clinical team.
Responsibilities
- Act as the primary point of contact for interpretation platform vendor(s), define requirements, and oversee implementation
- Maintain the end-to-end variant interpretation strategy, aligning with CLIA, CAP, and NYS requirements, and collaborate with Lab Director and clinical team
- Assist in validation of interpretation platform and laboratory processes for variant interpretation
- Assist with curation and harmonization of variant classification changes over time
- Perform secondary review of sequencing (Sanger, WGS) and other molecular data
- Assist in clinical interpretation for proactive health and rare disease applications, including evaluation of published literature and clinical data
- Master's Degree or PhD in molecular genetics, human genetics, or a related biological sciences field
- 2+ years of significant and relevant experience including variant classification in the context of rare disease and/or proactive health
- Strong analytical skills and ability to interpret data from scientific publications
- Strong communication, organizational, and interpersonal skills
- Ability to work independently
- Location: Remote-friendly with preference for Bay Area or Eastern time zones. Occasional travel required for team meetings.
- Compensation: $100-150K/year depending on experience; equity; and the following benefits:
- Company-paid health/vision/dental benefits
- 401K
- Unlimited PTO
- Company-sponsored offsites and team meals during in-person meetings
- Direct access to company leadership and opportunity to grow into an operational leadership role
Join us if you:
- Want to make an impact at the intersection of healthcare and technology, changing the way people engage with their health at the genetic level
- Enjoy rolling up your sleeves, taking initiative, and being empowered to lead
- Value humility, transparency, and collaborative problem-solving
- Thrive in fast-moving, dynamic environments with smart, driven teammates
- Appreciate competitive compensation, meaningful equity, and excellent benefits
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