Reporting Clinical Laboratory Scientist (contractor)

BillionToOne • Union City, CA

5d • Hybrid

About The Position

The Prenatal Reporting Clinical Laboratory Scientist (RCLS) contractor performs high-complexity clinical laboratory data analysis, reviews and interprets molecular diagnostic and sequencing results, and ensures accurate, reliable, and timely patient-result reporting in accordance with laboratory procedures and applicable regulatory requirements. The RCLS independently executes validated bioinformatics pipelines, evaluates analytical results and quality control metrics, troubleshoots issues, and reviews and releases clinical reports within established authorization and reporting procedures. Complex or unusual results may require collaboration with Bioinformatics, Laboratory Directors, and other clinical personnel.

The role also provides technical leadership through scientific judgment, investigation of complex analytical issues, guidance and training for colleagues, and identification of process improvements. The RCLS collaborates with Laboratory Operations, Bioinformatics, Quality Assurance Management, Genetic Counselors, Laboratory Directors, and other cross-functional teams to resolve technical challenges and support efficient laboratory workflows. The position requires attention to detail, analytical and problem-solving skills, strong communication, initiative, accountability, adaptability, and the ability to manage competing priorities independently and collaboratively.

This is a hybrid role requiring approximately 60% on-site presence at the Union City and/or Menlo Park offices: three days per week on-site and two days per week remote. The target hourly rate is $65.

Requirements

• Active, valid California CLS or Clinical Genetic Molecular Biologist Scientist (CGMBS) license, or an appropriate license to practice medicine, osteopathy, or podiatry under the specified California Business and Professions Code provisions and appropriate to the specialty performed.
• Bachelor's degree or higher in Biomedical Laboratory Sciences, Clinical Laboratory Science, Molecular Biology, Genetics, or a related scientific discipline, consistent with applicable licensure requirements.
• At least one year of clinical laboratory experience or equivalent experience in a high-complexity, high-volume molecular diagnostic clinical laboratory environment.
• Working knowledge of molecular biology principles, clinical laboratory testing methodologies, and applicable local, state, and federal laboratory regulations.
• Experience analyzing sequencing data, including evaluation and interpretation of next-generation sequencing results and associated analytical quality control metrics under validated laboratory procedures.
• Ability to independently analyze complex laboratory data, investigate discrepancies, and troubleshoot issues affecting test performance or reporting accuracy.
• Familiarity with bioinformatics analysis outputs and their application to clinical molecular diagnostic reporting.
• Strong computer skills and ability to use laboratory data management systems and analytical software effectively.
• Proficiency with Atlassian Suite, Google Workspace, and Microsoft Office Suite.
• Strong analytical judgment, attention to detail, organizational and problem-solving skills, and commitment to accurate, reliable clinical reporting.
• Ability to independently manage reporting responsibilities, prioritize competing demands, and adapt to operational needs while maintaining quality and turnaround time expectations.
• Initiative and accountability in investigating technical issues, identifying solutions, and exercising judgment about consultation and escalation.
• Excellent written and verbal communication skills and ability to provide technical guidance and collaborate across multidisciplinary teams.
• Receptiveness to feedback and commitment to continuous learning, professional development, and process improvement.

Responsibilities

• Execute established and validated bioinformatics pipelines to process and analyze molecular diagnostic data from patient samples.
• Review and interpret clinical genomic data, sequencing results, bioinformatics outputs, and quality control metrics against laboratory standards and reporting criteria.
• Identify, investigate, and troubleshoot analytical discrepancies, unusual findings, and data quality issues, collaborating with technical teams as needed.
• Manage daily sample analysis priorities, monitor workflows, and communicate technical issues that could affect accuracy or turnaround times.
• Review, verify, and release clinical laboratory reports according to established procedures, authorization, and regulatory requirements.
• Collaborate with RCLSs, Bioinformatics, Genetic Counselors, Laboratory Directors, and other clinical personnel to evaluate complex findings and resolve reporting discrepancies.
• Ensure clinical reports are accurate, complete, and consistent while meeting quality standards and turnaround time expectations.
• Document analytical reviews, quality assessments, investigations, and reporting decisions accurately.
• Communicate reporting concerns and unresolved issues to appropriate personnel promptly.
• Exercise sound scientific judgment and independently investigate analytical discrepancies and technical issues.
• Provide technical guidance to Reporting CLS colleagues and support consistent use of analytical and reporting procedures.
• Assist with training, onboarding, and mentoring Reporting CLS personnel and other clinical laboratory staff.
• Identify opportunities to improve reporting accuracy, workflow efficiency, and laboratory performance.
• Participate in technical leadership activities, investigations, validation projects, and workflow improvements as assigned.
• Perform and support quality control and quality assurance activities.
• Ensure compliance with CLIA, CAP, California state regulations, and laboratory policies and procedures.
• Document and investigate quality issues, nonconforming results, and procedural deviations.
• Support root cause investigations, corrective and preventive actions, and continuous quality improvement with Quality Management and laboratory leadership.
• Recommend analytical workflow, reporting accuracy, operational efficiency, and cost-effectiveness improvements.
• Collaborate on development, validation, implementation, and optimization of laboratory tests, methodologies, and reporting workflows.
• Assist with technology transfer and implementation of validated methodologies from Process Engineering into the clinical laboratory.
• Support evaluation and implementation of improvements to laboratory data management and reporting systems.
• Maintain and update reporting procedures, technical documentation, and workflow resources.
• Investigate recurring analytical or workflow issues and contribute to solutions.
• Collaborate across Laboratory Operations, Bioinformatics, Genetic Counseling, Client Services, Quality Assurance Management, and Process Engineering to resolve sample-specific and workflow issues.
• Communicate analytical findings, technical concerns, and recommended solutions to stakeholders.
• Serve as a technical contact for cross-functional teams on clinical reporting questions and analytical troubleshooting, as appropriate.
• Support laboratory leadership with reporting priorities, operational coordination, and project deliverables.
• Contribute to cross-functional initiatives that improve laboratory efficiency, reporting reliability, and operational performance.

Benefits

• Daily on-site lunches provided from top eateries.
• On-campus amenities including a state-of-the-art gym and restaurant.
• Free on-site EV charging compatible with all EVs, including Tesla.
• Opportunity to work with colleagues toward the company's global vision and contribute to molecular diagnostics that may help patients.

What This Job Offers

• Career Level: Mid Level