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Director Variant Analyst Jobs in California (NOW HIRING)

Senior Engineer

Alameda, CA

$118K - $162K/yr

Experience in precision analog signal chain analysis: error budget, dynamic range, analog and ... Must be self-motivated, well organized, and productive with minimal direct supervision * Excellent ...

Director of E-Commerce Marketing Come grow with us! Working at ViewSonic is a unique opportunity to ... Own marketplace analytics and reporting (e.g., Intentwise, Kapoq): weekly performance readouts ...

Senior Growth Product Manager

San Jose, CA

$148K - $195K/yr

Use AI to speed up experiment ideation, hypothesis generation, copy/variant drafting, and analysis ... direct authority * Strong stakeholder management skills, with experience aligning multiple teams ...

Showing results 21-40

Director Variant Analyst information

What are the key skills and qualifications needed to thrive as a director variant analyst, and why are they important?

To thrive as a Director Variant Analyst, you need advanced expertise in genomics, variant interpretation, and bioinformatics, often supported by a PhD or equivalent experience in genetics or molecular biology. Familiarity with next-generation sequencing (NGS) platforms, variant annotation tools, and clinical databases, along with relevant certifications such as board certification in clinical molecular genetics, is highly valued. Strong leadership, decision-making, and communication skills are critical for managing teams and collaborating across departments. These competencies ensure accurate and efficient analysis of genetic data, drive innovation, and support high-quality clinical or research outcomes.

What is a director variant analyst?

A Director Variant Analyst is a senior professional responsible for overseeing the analysis and interpretation of genetic variants within an organization, typically in a clinical or research genetics setting. They lead teams that evaluate genetic data to determine the clinical significance of DNA sequence variations, which is crucial for diagnosing genetic disorders or informing personalized medicine. The director collaborates with scientists, clinicians, and laboratory staff to ensure the accuracy and quality of genetic variant analysis and reporting. They may also contribute to the development of protocols, implementation of new technologies, and compliance with industry regulations. This role requires deep expertise in genetics, bioinformatics, and leadership.

What is the difference between Director Variant Analyst vs Variant Analyst?

AspectDirector Variant AnalystVariant Analyst
CredentialsBachelor's degree, often with experience in data analysis or geneticsBachelor's or higher in biology, genetics, or related field
Work EnvironmentLeadership role in labs or healthcare companies, overseeing projectsHands-on data analysis in labs or research settings
Industry UsageUsed in biotech, healthcare, and research organizationsCommon in genetics labs, research institutions, and healthcare

The main difference is that the Director Variant Analyst typically holds a leadership position with strategic responsibilities, while the Variant Analyst focuses on data analysis and research tasks. Both roles require relevant credentials and are integral to genetics and healthcare industries, but the Director role involves overseeing teams and projects.

What are the main challenges a director variant analyst faces when leading a genomics team?

A Director Variant Analyst often navigates challenges such as managing diverse teams of bioinformaticians and geneticists, ensuring data accuracy amidst rapidly evolving technologies, and balancing project deadlines with regulatory compliance. They must facilitate effective communication between research, clinical, and IT departments, especially when interpreting and reporting complex genomic data. Additionally, staying current with advancements in variant interpretation and integrating new tools while maintaining operational efficiency is a key aspect of the role.
What are the most commonly searched types of Variant Analyst jobs in California? The most popular types of Variant Analyst jobs in California are:
What job categories do people searching Director Variant Analyst jobs in California look for? The top searched job categories for Director Variant Analyst jobs in California are:
What cities in California are hiring for Director Variant Analyst jobs? Cities in California with the most Director Variant Analyst job openings:
Infographic showing various Director Variant Analyst job openings in California as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 3% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Senior Product Manager, Sightline

Verily Life Sciences

San Bruno, CA โ€ข On-site

$151K - $199K/yr

Full-time

Posted 22 days ago


Job description

Who We Are
Verily Health is a data platform and technology company purpose-built to power AI-enabled precision health solutions that accelerate research and improve care for individuals and communities. Uniquely positioned at the intersection of technology, data science, and healthcare, Verily transforms multimodal health data into insights, models, and actions that make healthcare more personalized, predictive, and precise.
Description
As a Sightline Product Manager, you will drive day-to-day execution for Verily's flagship population health intelligence platform. This role focuses on commercializing predictive analytics and accelerating our transition into a high-margin data insights business. You will shepherd the platform lifecycle as we scale multi-modal forecasting tools, expand into advanced microbiome sequencing, and capture international markets.
This is an execution-focused position requiring a precise intersection of scientific insight and agile program mastery. Leveraging your background in infectious disease, you will translate complex biological workflows into engineering directives. Using your strong background as a Product Manager and certified Agile practitioner, you will maintain sprint velocities and pipeline tracking to deliver world-class science to our life sciences, biosecurity, and public health partners.
Responsibilities
  • Drive Commercial Product Strategy: Translate complex pharma and biosecurity workflows into clear product requirements and user stories for high-value predictive analytics, forecasting, and variant horizon-scanning tools.
  • Scale Molecular Diagnostic Pipelines: Serve as the core translation layer for engineering and computational biology teams to scale routine digital PCR (ddPCR), amplicon sequencing, and next-generation metagenomic sequencing (mNGS) workflows.
  • Champion Technical Agile Execution: Run daily Scrum ceremonies and own JIRA/Confluence roadmapping from design to production-grade deployment for dedicated software and computational biology squads.
  • Facilitate Ecosystem Integration: Coordinate data integration frameworks across broader public health endpoints and centralized data marketplaces to achieve continuous product parity.
  • Manage Data Governance & IP: Collaborate with clinical, legal, and academic stakeholders to safely navigate complex technical sample transfer protocols, intellectual property, and data licensing guidelines.

Qualifications
Minimum Qualifications
  • Experience: 3+ years of demonstrated work experience as a Product Manager, Technical Project Manager, or Technical Product Manager leading platform execution in a life sciences, biotech, or high-tech environment.
  • Educational Background: Degree (B.S., M.S., or Ph.D.) or practical professional experience in Computational Biology, Bioinformatics, Genomics, or a related quantitative life sciences discipline.
  • Domain Expertise: A background in infectious disease (e.g., exposure to epidemiology, molecular diagnostics, public health surveillance, or virology).
  • Technical Operational Depth: Deep familiarity with JIRA ticketing systems, managing data engine deployment cycles, and holding cross-functional squads accountable to delivery timelines.
  • Complex Stakeholder Communication: Proven ability to translate intricate scientific data parameters (such as assay configurations, signal-to-noise ratios, and variant abundances) into structured, scannable technical requirements for platform engineers.

Preferred Qualifications
  • Agile Certification: Active, industry-recognized certification (e.g., CSM, CSPO, PMP-ACP, or SAFe).
  • Direct experience working with high-throughput laboratory data architectures (such as ddPCR data strings, amplicon sequencing, or raw genomic sequence datasets).
  • Familiarity with the biopharma value chain, specifically how population-level biological insights optimize vaccine strain selection and clinical trial recruitment timelines.

The US base salary range for this full-time position is $140,500 - $210,500 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.
Verily Health Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here.
If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.