Lead a global software engineering team in the women's health domain while actively contributing to code, architecture, and testing. Drive AI transformation within the team's workflow to improve delivery, quality, and compliance in a regulated environment.
The manager will lead complex FDA regulatory submissions for biologic programs and oversee quality systems including CAPA and SOP management. They will provide regulatory guidance to cross-functional teams to ensure compliance and facilitate rapid product approvals.
The Revenue Cycle Medical Records Case Manager supports medical necessity documentation by facilitating record collection and client outreach. They serve as a liaison between billing operations and clinical departments while interpreting complex medical data to support revenue cycle performance.
The Senior Product Manager will lead the strategy and development of physician-facing real-world evidence (RWD) applications to improve treatment outcomes and clinical workflows. This role involves collaborating with cross-functional teams, including AI/ML and clinical experts, to integrate genomic data and patient insights into actionable tools for healthcare providers.
The Senior Forward Deployed Data Engineer will design, build, and deploy high-impact analytics and AI solutions by partnering directly with business stakeholders. They will write production-grade code, develop semantic layers, and implement agentic workflows to turn clinical and genomic data into actionable products.
Lead the research, development, and clinical translation of AI and computational algorithms for oncology diagnostics. Build and manage a high-performing algorithm team while setting strategy for foundation models and multimodal product development.
Lead the clinical and scientific aspects of sponsored clinical studies, ensuring patient safety, data integrity, study quality, and progress against timelines and budgets. Contribute to program strategy, interpret study data, manage cross-functional and external stakeholder relationships, and represent the clinical function in internal and external discussions.
Lead research on machine learning and deep learning models using NGS data to drive the development of Women's and Organ Health products. Collaborate with cross-functional teams to design experiments, build bioinformatics pipelines, and contribute to the company's intellectual property portfolio.
The Research Associate will manage biological samples, ensuring their integrity through proper collection, processing, and storage protocols. They will also maintain sample databases, perform quality control, and collaborate with research teams to support scientific projects.
Lead and mentor a shift team to ensure timely resolution of production data analysis tickets while fostering a culture of accountability and innovation. Represent the team in stakeholder meetings, manage operational effectiveness, and provide career development for team members.
The Senior Data Analyst will provide critical data analytics support for lab production operations, including diagnosing operational issues and improving turnaround times. They will also design automated solutions for recurring workflows and collaborate with cross-functional teams to drive continuous improvement.
Lead the design, analysis, and interpretation of R&D and analytical validation studies for molecular diagnostic tests. Effectively communicate statistical concepts to cross-functional teams and provide technical supervision to junior staff.
The Associate Director, Tax will manage federal, state, and international tax compliance, including income, sales, and use tax filings. They will also develop strategic tax planning initiatives and oversee process improvements to ensure accurate reporting and risk mitigation.
The Inside Sales Manager leads the inside sales team to develop strategies that support field sales and grow the customer base. They are responsible for overseeing daily activities, coaching team members, and reporting performance metrics to senior management.
Drive technical workstreams to develop and validate novel machine learning methods for early cancer detection using cfDNA methylation data. Collaborate with molecular biologists on experimental design while providing technical leadership and mentorship to the team.
You will build and maintain SMART on FHIR applications and CDS Hooks services that integrate Natera's diagnostic tools directly into clinician EHR workflows. This role involves managing patient data securely under HIPAA compliance and collaborating with health system IT teams for successful go-live deployments.
Develop, train, and evaluate machine learning models to support cancer detection in the minimal residual disease setting. Manage end-to-end research analyses from ideation through implementation while ensuring high-quality standards for sequencing data.
Lead a Data Engineering & Delivery team to develop and maintain robust data infrastructure, ETL pipelines, and data products for production support. Collaborate with cross-functional stakeholders to align development roadmaps and ensure the efficient delivery of data systems that meet business needs.
The Patient Coordinator manages patient relationships and drives revenue through proactive outreach and pipeline development. They collaborate with cross-functional teams to ensure timely testing and provide consultative support to patients throughout the sales process.
The Associate Director/Director will own the product strategy and roadmap for Signatera in hematologic malignancies, managing the lifecycle from market entry to clinical trial support. They will collaborate across a matrixed organization to define product requirements, drive evidence generation, and lead launch readiness initiatives.
Lead clinical development strategy and the design and execution of oncology studies for early cancer detection and cfDNA IVD products, including protocols, regulatory materials, data reviews, and safety oversight. Coordinate with investigators, CROs, internal teams, senior leaders, and external clinical partners to deliver high-quality study data and meet program milestones.
Lead complex IVD and companion diagnostic programs from development planning through PMA submission. Integrate cross-functional workstreams including assay development, regulatory affairs, and clinical validation to drive program milestones.
The manager will lead a team of bioinformaticians and data scientists in the design, development, and validation of ctDNA-based diagnostic tests. They are responsible for optimizing analysis pipelines, managing technical resources, and ensuring high-quality documentation for commercial product launches.
Drive sales growth and adoption of Signatera molecular diagnostic tests by developing strategic partnerships with academic and community oncology stakeholders. Manage territory business plans to maximize revenue, improve account performance, and collaborate cross-functionally to support customer success.
Lead bioinformatics and real-world evidence analyses across large-scale genomic, clinical, and healthcare datasets, integrating multimodal data and applying AI/ML methods to identify clinical insights, predict outcomes, and discover biomarkers. Manage projects from planning through delivery, collaborate across technical and clinical teams, and communicate findings through visualizations, reports, and publications.
The Data Privacy Director will lead the enterprise privacy program by operationalizing privacy-by-design across product, clinical, and commercial environments. This role involves managing privacy impact assessments, data governance frameworks, and cross-functional collaboration to ensure responsible data use and regulatory compliance.
The Staff Biostatistician will lead the design, analysis, and interpretation of clinical validation studies to support regulatory approvals for molecular diagnostic products. They will also serve as a statistical lead on cross-functional teams, ensuring compliance with FDA standards and mentoring junior staff.
Lead development, design verification, and validation of NGS-based early cancer detection IVD products, including analytical performance studies and data packages for FDA Class III PMA submissions. Direct and develop scientific teams, coordinate cross-functional and commercial-lab transfers, manage technical risks and budgets, and serve as a technical expert in FDA interactions.
Own the multi-year development strategy and phase-gated execution of NGS- and cfDNA-based early cancer detection products, from feasibility through FDA approval and post-market support. Lead teams and resource planning, guide analytical and clinical evidence development, represent development in FDA interactions, and ensure design controls and quality-system compliance.
The Sales Training Manager creates and delivers clinical and sales training content for the Oncology business unit while collaborating with cross-functional teams. They are responsible for coordinating onboarding experiences, developing training programs, and supporting sales professionals to ensure success in competitive markets.
