The Supervisor oversees daily operations and performance for the Prior Authorization teams, managing both domestic and offshore staff to ensure timely case resolution. This role drives operational improvements, monitors KPIs, and serves as an escalation point for complex authorization issues and payer disputes.
The Supervisor oversees daily operations for prior authorization teams, ensuring efficient workflow management and timely case resolution. They provide leadership and coaching to domestic and offshore staff while monitoring performance metrics to drive operational improvements.
The Oncology Trial Navigator manages patient matching workflows by screening clinical data and coordinating with oncologists and research sites to facilitate trial enrollment. They also provide clinical expertise to refine AI-enabled matching tools and offer empathetic support to patients throughout the referral process.
The Product Manager will drive the product roadmap for the end-to-end tissue acquisition journey to improve processes for patients, clinics, and pathology labs. They will collaborate with cross-functional teams to define requirements, prioritize backlogs, and deliver software solutions that streamline operations.
The Senior Regulatory Affairs Specialist prepares and manages regulatory submissions for medical and in vitro diagnostic devices to ensure compliance with domestic and international requirements. They also provide regulatory guidance to product development teams and interact with agencies like the FDA to secure market clearance.
The Regulatory Advisor develops and executes regulatory strategies for FDA Pharma and IVDR initiatives while representing the regulatory team on cross-functional projects. They are responsible for preparing regulatory submissions, maintaining product registrations, and ensuring compliance across labeling and promotional materials.
Support Clinical Field Specialists in closing sales, growing revenue, developing markets, and maintaining existing customer relationships with maternal-fetal medicine and OB/GYN professionals. Assess customer needs, coordinate logistics, resolve issues, support product launches, and maintain compliant, confidential, service-oriented customer interactions.
The Email Marketing Specialist plans, executes, and optimizes email campaigns to drive engagement and ROI. This role manages end-to-end production, including audience segmentation, email building, QA, and performance reporting.
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.
Review and interpret oncology pathology reports and clinical notes, curate clinical and specimen information in the Signatera database, and identify optimal samples for minimal residual disease testing. Advise internal teams and referring laboratories on specimen acquisition, diagnostic data organization, sample quality and timing, and clinical trial data transfer.
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 Regional Director will hire, lead, and develop a team of Clinical Oncology Specialists to drive the adoption of Signatera molecular residual disease tests across the Eastern United States. They are responsible for executing regional sales strategies, building relationships with key opinion leaders, and ensuring the team meets or exceeds commercial objectives.
The Finance Functional Lead will serve as the primary product owner for Oracle Fusion Financials, managing the roadmap, configuration, and delivery of finance initiatives. They will also govern offshore managed service partners and act as the key point of contact for senior finance leadership to ensure audit readiness and process optimization.
The Patient Coordinator acts as a patient advocate to manage testing logistics and support existing customers in collaboration with Nurse Coordinators. They are responsible for identifying and nurturing patient relationships to drive market development and ensure timely testing schedules.
You will own the strategy, roadmap, and backlog for Sales and Marketing platforms, ensuring Salesforce serves as the primary system of record for commercial workflows. You will partner with engineering and commercial stakeholders to translate business needs into measurable outcomes and prioritize initiatives based on value and impact.
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.
Lead and oversee statistical programming deliverables, including analysis datasets and tables, listings, and figures for regulatory submissions. Manage a team of statistical programmers while contributing hands-on to programming tasks and maintaining the statistical computing infrastructure.
You will own the architecture, implementation, and delivery of major platform initiatives while mentoring mid-level engineers. Additionally, you will partner with cross-functional teams to build AI-augmented tooling and translate scientific needs into scalable platform capabilities.
Lead the development of novel statistical and machine learning methods for cancer signal detection using multi-modal genomic data. Collaborate with molecular biologists and clinical experts to prototype, test, and productionize scalable models for clinical validation.
The Medical Science Liaison serves as a field-based scientific resource engaging clinicians and academic institutions to support Natera’s oncology products. Responsibilities include building relationships with key opinion leaders, providing scientific presentations, and supporting clinical trial initiatives.
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 pipelines and translate research prototypes into validated clinical tools.
The supervisor oversees day-to-day laboratory operations, including staffing, scheduling, and ensuring high-quality sample processing in compliance with regulatory standards. They also provide leadership to team members, manage performance, and collaborate with management to resolve operational issues and improve processes.
The role involves driving commercial strategy and execution for breast cancer products while leading cross-functional teams to define key indications and evidence roadmaps. The individual will also manage KOL relationships, develop value propositions, and collaborate with market access to secure reimbursement.
The Organ Health Specialist will drive revenue growth and market adoption of transplant-focused diagnostic and genetic testing solutions within a designated territory. This involves cultivating relationships with key opinion leaders and transplant specialists to integrate products like Prospera and Renasight into clinical practice.
Drive the adoption and growth of the Signatera MRD assay by building strategic relationships with oncologists and multidisciplinary care teams. Develop and execute territory plans to identify growth opportunities and achieve sales objectives within the assigned region.
The manager will lead and mentor an extended-hours support team to provide timely data analytics services for lab production operations. They are responsible for ensuring operational excellence, managing stakeholder expectations, and driving process improvements through automation and innovation.
The Director will build and lead the bioinformatics function, defining strategy and vision for genomic algorithm development. They will also architect scalable AWS infrastructure and implement MLOps to ensure reliable deployment of clinical products.
The scientist will lead the development, optimization, and validation of IHC and tissue-based workflows for oncology products. They will collaborate with cross-functional teams to transfer R&D methods into robust clinical laboratory workflows.
The Tech Lead will set the technical direction for a solutions team, owning the architecture and design of analytics and AI pipelines. They will also mentor engineers, enforce engineering standards, and partner with business stakeholders to deliver scalable data products.
The Area Medical Director serves as the primary clinical lead for the community oncology market, driving scientific engagement and regional medical strategy. This role involves cross-functional collaboration with sales and marketing teams to accelerate the utilization of the oncology portfolio while surfacing clinical intelligence.
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.
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 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.
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 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 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.
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.
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.
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.
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.
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.
