The analyst will lead cross-functional process improvements and manage project objectives through collaboration and data-driven insights. They are responsible for auditing communications, tracking performance KPIs, and maintaining documentation to ensure quality standards are met.
The Senior Accountant will manage clinical trial accruals, R&D expense analysis, and month-end close activities in compliance with GAAP and SOX. They will partner cross-functionally with Clinical Operations and FP&A to ensure accurate financial reporting and process improvements.
Lead a Data Engineering & Delivery team to develop and maintain robust data infrastructure, ETL pipelines, and data delivery solutions. Manage team operations, ensure compliance with quality standards, and collaborate with cross-functional stakeholders to align development roadmaps.
The Inside Sales Manager will strategically lead the inside sales team to support field sales, drive lead generation, and achieve sales objectives. They are responsible for coaching team members, developing sales scripts, and reporting on performance metrics to senior management.
Lead a DevOps team to develop, deploy, and maintain data and cloud platforms while ensuring efficient software delivery. Collaborate with cross-functional stakeholders to align infrastructure roadmaps and maintain high-performance, compliant systems.
Provide genetic counseling to patients via telephone and video while reviewing medical histories and explaining genetic risks. Assist in the development of clinical protocols and support various internal teams including lab genetic counselors and medical science liaisons.
The Account Manager is responsible for driving the adoption and growth of Natera’s oncology testing portfolio by collaborating with local distributors and healthcare providers. They will develop territory strategies, execute sales initiatives, and provide ongoing education to ensure high customer satisfaction.
You will identify, design, and deploy AI-driven automation workflows to enhance business efficiency across various domains. You are responsible for end-to-end agent performance, including monitoring KPIs, managing observability, and ensuring reliable integration with enterprise systems.
The genetic counselor will serve as a clinical liaison to patients and providers, reviewing oncology test results and providing genetic information sessions. They will also assist in lab operations, develop patient education materials, and collaborate on scientific abstracts.
Direct and mentor a team of data science support engineers to provide timely analytics for production teams within a regulated environment. Lead the team during critical production incidents and manage infrastructure for operational visibility and efficiency.
The supervisor will manage a team dedicated to executing billing strategies, monitoring performance KPIs, and ensuring accurate insurance verification and collections. They are also responsible for staff development, training, and acting as the first point of escalation for patient concerns.
The Account Manager is responsible for driving the adoption and growth of Natera's oncology testing portfolio by collaborating with local distributors and healthcare providers. They will develop territory strategies, execute sales initiatives, and provide ongoing education to surgeons, oncologists, and hospital staff.
The Team Lead oversees daily phlebotomy operations, ensuring compliance, quality assurance, and effective team management. They also facilitate cross-functional collaboration and provide support for audits and onsite visits.
The Director will build and lead the bioinformatics function, defining strategy and technical roadmaps for genomic algorithm development. They will also architect scalable AWS infrastructure and ensure the quality and reproducibility of clinical production pipelines.
The Medical Science Liaison serves as a field-based scientific resource for clinicians and academic institutions, providing clinical presentations on genetics and organ health. They also manage interactions with Key Opinion Leaders and provide scientific support to internal sales and marketing teams.
The Senior Area Marketing Manager will develop and execute regional marketing initiatives and campaigns to drive the adoption of genetic tests among healthcare providers. They will collaborate with sales and medical affairs teams to manage regional programs, analyze campaign ROI, and gather customer insights.
The Clinical Field Specialist drives revenue growth and market expansion by providing clinical insight and technical training to OB/GYNs and MFMs. They are responsible for executing strategic business plans and cultivating key relationships within their assigned territory.
The Oncology Pathology Assistant serves as a subject matter expert for clinical pathology reports and assists in the acquisition of specimens for minimal residual disease testing. They are responsible for curating clinical data, maintaining diagnostic records, and supporting various internal teams including medical, sales, and clinical trials.
The Director of Alliance Management will serve as the primary relationship owner for key BioPharma partners, providing governance and strategic alignment throughout the partnership lifecycle. They will also lead portfolio-level execution across clinical and diagnostic initiatives while driving horizontal partnership expansion.
Lead and mentor a team of bioinformatics scientists to drive research strategy and assay development for women's and organ health diagnostic projects. Oversee the transition of research prototypes into stable, production-ready pipelines while ensuring high standards of data quality and scientific rigor.
The Lead Bioinformatician will develop and implement algorithmic foundations for diagnostic assays, focusing on detecting variants in challenging cfDNA samples. They will also serve as a genomics consultant for production escalations and collaborate cross-functionally to ensure data quality and system integration.
You will lead a team of scientists to manage production support for bioinformatics and data science algorithms, ensuring accurate and timely results. This role involves investigating complex system issues, defining process validation standards, and partnering across departments to resolve operational challenges.
The Senior Manager is responsible for managing all aspects of clinical trials, including study design, protocol implementation, and site monitoring. They also oversee clinical research staff, manage study budgets, and coordinate with CROs and investigative sites.
The Medical Science Liaison will serve as a scientific expert, engaging with oncology healthcare providers to share clinical data and educate on molecular diagnostics. They are responsible for building key opinion leader relationships and gathering actionable field insights to support medical affairs initiatives.
The Organ Health Specialist will drive market adoption of Natera's genetic testing products by cultivating relationships with nephrology providers and executing strategic business plans. They are responsible for achieving sales goals and serving as a local technical expert within their assigned territory.
The Principal, Pharmacovigilance / Device Vigilance supports safety surveillance for diagnostic and software-driven products throughout their lifecycle. This role manages adverse events, product complaints, and regulatory reporting to ensure compliance with global standards such as FDA and EU IVDR.
The Staff Scientist will lead the analysis of large-scale multi-omics and real-world data to extract actionable clinical insights using AI and machine learning methodologies. They will oversee end-to-end research projects and collaborate cross-functionally to integrate genomic data into clinical and regulatory strategies.
The manager will lead training initiatives across multiple departments by leveraging AI and data analytics to identify skill gaps and improve performance. They are responsible for designing, executing, and measuring the effectiveness of onboarding and continuous development programs.
The Oncology Pathology Assistant will review clinical pathology reports to identify optimal specimens for minimal residual disease testing and ensure accurate data entry into the sample database. They will serve as a subject matter expert for internal teams, including medical, customer service, and clinical trial departments.
The Medical Science Liaison will establish scientific relationships with oncology healthcare providers and deliver clinical education on Natera's molecular diagnostics. They are responsible for identifying field insights and supporting medical affairs initiatives while ensuring compliance with company policies.
You will identify and build AI-driven automation workflows to enhance business efficiency across various domains. You are responsible for deploying these agents into production, monitoring their performance via KPIs, and ensuring they integrate reliably with enterprise systems.
Review pathology tissue samples for accuracy and completeness using LIMS and clinical notes for Signatera and Altera testing. Collaborate with team members to resolve discrepancies and ensure timely resolution of non-conforming samples.
Design and deploy agent-based AI systems to improve the quality and reliability of clinical data extraction within a production pipeline. Partner with cross-functional teams to define success metrics and implement scalable AI capabilities in a regulated healthcare environment.
Serve as the primary technical owner of the Workday platform, managing configuration, integrations, security, and release management across HCM, Payroll, and Recruiting. You will translate business requirements into technical delivery plans and build custom applications using Workday Extend.
Lead the development and optimization of bioinformatics pipelines for ctDNA-based diagnostic tests in oncology. Manage a team of bioinformaticians and data scientists while collaborating cross-functionally to move products from research to commercial launch.
Lead the technical aspects of pre-sales and customer discovery, focusing on EHR integrated digital engagement and clinical care pathway optimizations. Act as a technical liaison between sales, product, and engineering teams to manage RFPs and pilot implementations.
Establish and maintain scientific relationships with oncology healthcare providers and key opinion leaders to deliver education on molecular diagnostics. Act as a subject matter expert to share clinical data and provide actionable field insights to improve disease management.
The phlebotomist is responsible for retrieving blood specimens via venipuncture and ensuring specimen integrity through aseptic techniques. They also manage logistical tasks including tracking draws in Skedulo, handling patient reports, and coordinating courier pickups.
The phlebotomist is responsible for identifying the best blood retrieval methods, performing venipunctures, and preparing specimens for laboratory testing. They must also manage logistical tasks such as updating job statuses in Skedulo and coordinating courier pickups.
Lead the strategy, development, and lifecycle management of the Early Cancer Detection product portfolio from concept to launch. Manage a high-performing product management team and collaborate with cross-functional departments to drive business and patient outcomes.
The Alliance Manager leads strategic external oncology partnerships to integrate Natera's technology into drug development pipelines. They oversee study intake, manage legal coordination for contracts, and ensure strategic objectives are translated into operational plans.
Lead the clinical development and medical strategy for molecular diagnostics in genitourinary cancers. This includes designing clinical studies, engaging key opinion leaders, and providing medical affairs support to drive the adoption of precision oncology tools.
Oversee the design, analysis, and interpretation of clinical trials for regulatory submissions within the oncology portfolio. Lead the execution of statistical analyses and mentor junior team members while communicating results to cross-functional stakeholders.
Drive the adoption of Natera's oncology portfolio by navigating complex academic health systems and bridging the gap between medical and surgical oncology. Collaborate cross-functionally to execute strategic account plans and optimize clinical workflows for patient testing.
Lead a team of Laboratory Systems Scientists to implement and optimize laboratory systems and operational processes. Bridge strategic direction with day-to-day execution across process engineering, asset management, and technology transfer to ensure scalable and compliant workflows.
Own the end-to-end architecture and delivery of Natera's production Voice AI platform for patient interactions. Design and implement multi-agent conversational systems, real-time audio pipelines, and observability infrastructure to improve patient access to genetic testing results.
Design, build, and deploy AI agents and automation pipelines to enhance efficiency across various business domains. Own the end-to-end performance of these systems, including monitoring KPIs, managing evals, and iterating on workflows in production.
Direct medical strategy and clinical development for cfDNA and liquid biopsy portfolios focusing on gynecologic malignancies. Collaborate across R&D, commercial, and medical affairs to drive clinical adoption and evidence generation for molecular testing solutions.
Develop and execute strategies to increase Natera testing within IDNs, large hospital systems, and Academic Medical Centers in the New England area. Collaborate with internal teams and external stakeholders to implement EMR tools and recruit strategic lab partners.
Own the full architecture, implementation, and delivery of large-scale cloud infrastructure and data platforms for R&D. Lead technical design reviews, mentor mid-level engineers, and develop AI-augmented coding tools to increase team productivity.
Lead the architecture and validation of genomic and multimodal foundation models to accelerate patient stratification and therapeutic monitoring. Bridge the gap between AI research and clinical science to transition representation learning models into reproducible diagnostic assets.
Define and drive the multi-year product strategy for the Results, Interpretation, and Reporting (RIR) platform to support complex genomics workflows. Lead cross-functional alignment between engineering, clinical, and regulatory teams to ensure scalable and compliant software systems.
Lead and scale a regional team of translational scientists to manage data collaborations and investigator-led trials within the Oncology Business Unit. Act as the executive authority for advanced molecular tests and translate field-derived real-world evidence into pipeline recommendations.
The Principal Clinical Scientist will lead the execution and design of multi-cancer early detection clinical studies while driving cross-functional collaboration. They are responsible for analyzing complex clinical datasets to provide actionable insights and ensuring the integrity of study performance.
The Regional Medical Director will lead clinical strategy and evidence generation for melanoma and immunotherapy applications, collaborating with various teams to ensure clinical adoption of oncology testing solutions. They will also serve as a spokesperson for skin and immuno-oncology programs, providing education and strategic guidance to healthcare providers and stakeholders.
