The analyst will monitor claim status activity, identify barriers to claim acceptance, and drive resolution through process improvement and automation. They will serve as a subject matter expert for EDI transactions and collaborate with cross-functional teams to optimize revenue cycle performance.
Lead and mentor a team of Bioinformatics Scientists to drive research strategy and assay development for diagnostic projects. Oversee the transition of research prototypes into stable, production-ready pipelines while ensuring high standards of data quality and scientific rigor.
Perform high-quality medical record abstraction by interpreting and managing complex clinical patient data for research and regulatory reporting. Utilize specialized data management software to ensure data integrity and support cross-functional teams in clinical encoding requirements.
The Product Manager will own the product roadmap and backlog for LIMS software, translating business and clinical requirements into executable technical specifications. They will collaborate with cross-functional teams including engineering, design, and lab operations to develop and deliver high-quality software solutions.
The Lead Biostatistician will independently design, analyze, and report on oncology clinical trials while providing technical expertise for study planning. They will collaborate with cross-functional teams to ensure high-quality statistical deliverables and mentor early-career staff.
The Principal Biostatistician will lead the statistical design, analysis, and reporting for oncology randomized control clinical trials. They will also mentor junior team members and collaborate cross-functionally to drive innovation in study methodologies.
The Associate Medical Director executes field engagement activities, supports MSL partnerships, and delivers scientific education within assigned regional accounts. They also contribute to insight generation, clinical development support, and cross-functional coordination to ensure high-quality medical affairs execution.
The Client Billing Specialist is responsible for ensuring accurate and timely billing of services while maintaining collaborative relationships within the revenue cycle management team. They will analyze billing trends, resolve billing issues, and implement process improvements to enhance overall performance.
The Senior Software Engineer will lead the design, development, and maintenance of backend microservices for commercial order processing systems. They will also mentor engineering staff, drive technical best practices, and collaborate with product managers to support the full software development lifecycle.
The Medical Science Liaison will establish scientific relationships with GI oncology healthcare providers and deliver clinically relevant education on Natera's molecular diagnostics. The role involves gathering field insights, supporting medical affairs initiatives, and coordinating clinical research activities.
The Senior Program Manager leads complex, cross-functional product development programs from early development through clinical trial launch and regulatory submission. They are responsible for driving milestones, managing risks, and ensuring alignment across R&D, Software, Quality, Regulatory, and Operations teams.
Design, build, and deploy agent-based AI systems to improve the quality and reliability of clinical data extraction in production. Collaborate with clinical AI, engineering, and product teams to define success metrics and integrate new AI capabilities into existing platforms.
The Organ Health Specialist will drive revenue growth and market adoption of transplant-focused diagnostic and genetic testing solutions within assigned territories. This role involves cultivating relationships with transplant specialists and key opinion leaders to integrate products like Prospera and Renasight into clinical practice.
The Customer Experience Associate manages interactions with patients and medical professionals to process test samples and resolve inquiries. They also support the sales team with account management, order tracking, and clinical inquiry triage.
The Senior Software Engineer will design, build, and maintain scalable microservices and web applications while mentoring the development team on best practices. They will collaborate with stakeholders and the architecture team to define requirements and ensure the delivery of reliable, high-quality software solutions.
Develop and deploy multimodal deep learning models integrating imaging, genomic, and clinical data to advance oncology diagnostics. Collaborate with cross-functional teams to scale machine learning workflows and translate prototypes into validated, production-quality tools.
Develop, train, and evaluate machine learning models to support cancer detection in the minimal residual disease setting. Manage end-to-end research analyses and communicate findings to both technical and cross-functional stakeholders.
The Regional Director is responsible for driving sales growth of genetic testing products by leading, recruiting, and coaching a team of sales professionals. They will develop regional strategies, manage territory alignments, and build relationships with key opinion leaders in the OBGYN community.
The Patient Coordinator will manage patient relationships to ensure timely testing and serve as a patient advocate within Natera. Responsibilities include collaborating with Nurse Coordinators to support customers, manage logistics, and drive market development.
The Associate Clinical Oncology Specialist is responsible for supporting oncology product sales, maintaining key account relationships, and ensuring patient adherence to prescribed testing protocols. They will analyze performance data and collaborate with internal stakeholders to improve clinical workflows and patient retention.
Lead the development and execution of health economic models and real-world evidence to demonstrate the clinical and economic value of precision diagnostics. Collaborate cross-functionally to integrate HEOR evidence into product lifecycle strategies, supporting market access, reimbursement, and commercialization.
You will lead the development and execution of health economic and outcomes evidence to demonstrate the value of precision molecular diagnostic technologies. This involves collaborating across cross-functional teams to integrate HEOR objectives into clinical studies and supporting market access and reimbursement strategies.
The Director of Corporate Compliance will serve as a strategic partner to Oncology leadership, providing risk-based guidance on commercial activities, clinical trials, and pharmaceutical collaborations. They are responsible for identifying emerging compliance risks, developing monitoring programs, and ensuring business initiatives align with federal and state healthcare regulations.
The Tax Manager is responsible for managing federal, state, and international tax compliance, including income, sales, use, and property tax filings. They will also develop strategic tax planning initiatives, oversee tax audits, and drive process improvements within the tax function.
Drive the product strategy and roadmap to improve patient engagement in longitudinal monitoring and simplify the testing experience for providers. Partner across commercial, operations, and engineering teams to ensure products reflect clinical workflows and meet business objectives.
The Manager, Clinical Trials oversees all aspects of clinical studies from start-up to close-out, ensuring compliance with protocols, budgets, and timelines. They manage CROs and vendors, lead study-related documentation, and provide leadership to clinical trial staff.
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.
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 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 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.
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 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 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.
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.
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 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.
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.
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.
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.
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.
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.
