I'm looking for a job. I exported this list from FewerJobs.com - a curated job board.

Please:
1. Rank these jobs by fit for me, given my resume / skills.
2. Highlight the top 5 with a one-sentence rationale each.
3. Flag any concerns, including benefit values without source-backed evidence.
4. Suggest one or two filter changes I could make on FewerJobs to find more good matches.

Filters I applied:
- q: Natera
- quality_floor: default
- match_401k_strict: true
- parental_strict: true
- non_birth_strict: true
- pto_strict: true
- include_older: false
- apply_url_verified: false
- page: 2
- per_page: 100
- sort: relevance

Jobs (67 total):

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TITLE: MLS Data Reviewer I
EMPLOYER: Natera
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-08
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6014628004
EXCERPT: MLS Data Reviewer I US Remote POSITION SUMMARY: The Medical Laboratory Scientist I, Data Reviewer is a member of the Operations Department to review and analyze clinical test results. This individual collaborates with a team of CLS and laboratory personnel to maintain accurate records of test results and patient information and perform any troubleshooting as needed. PRIMARY RESPONSIBILITIES: • Review clinical test results of molecular genetic testing received from laboratories for accuracy and translate intoLIMS • Review and analyze raw data files in proper software and resolve routine issues • Verify the proper specimen analyzed for patients and review the test requisition forms to verify the correct tests were performed. • Work within several laboratory information systems to review patient demographics and make corrections as needed • Responsible for understanding most current applicable standard operating procedures • Ensures compliance with all regulatory agency requirements through documentation, audits, and corrective action and follows GLP (good laboratory practice) • Comply with all company and department policies and procedures. This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job • Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training, and security training as soon as possible but not later than the first 30 days of hire • Performs other duties as assigned QUALIFICATIONS: • 0-2-years experience as an ASCP-certified Medical Technologist in a clinical laboratory
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TITLE: Clinical Lab Scientist I
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-28
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6006099004
EXCERPT: Clinical Lab Scientist I San Carlos, CA POSITION SUMMARY: The Clinical Laboratory Scientist analyzes specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: • Verify the proper specimen being analyzed and perform tests that need to be completed • Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors • Responsible for maintaining updated understanding and knowledge of methods performed in the lab • Follows GLP (good laboratory practice): maintain clean and organized work space • Completes training and other deadlines on time. • Go-to person when lead/supervisor is not available • Train on specialized instructions for instruments/protocols (super users) • Recognizes and escalates equipment malfunctions; troubleshoots common errors • Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor • Participates in the updating of departmental standard operating procedures and database to accurately reflect the current practices. • Ensures compliance with all regulatory agency requirements through proper documentation • Performs quality control procedures to ensure accuracy of clinical data (if applicable) • Maintains equipment and instruments in good operating condition • Communicates with team and other departments (including via e-mail) • Provides feedback on day-to-day schedule and tasks to lead/supervisor; offers suggestions/ideas for improvement • Assists teammates in completing daily tasks • Conducts himself/herself in a professional manner; acts as a role model/mentor to others • Adheres to Departmental Expectations • This role works with PHI on a regular basis both in paper and electronic form and have an
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TITLE: Manager, Clinical Trials
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $116K-$145K
POSTED: 2026-06-11
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6019281004
EXCERPT: Manager, Clinical Trials US Remote POSITION SUMMARY: The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES: - Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met - Responsible for selection of vendors/CROs and provide effective ongoing management to vendors/CROs working on the project to ensure compliance and execution of project deliverables within the approved budget, study timeline, and study protocol. Works closely with investigative site personnel, CROs, and other study vendors - Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites - Lead study-related activities such as protocol and informed consent preparation, investigator selection, study training material development and delivery, monitoring plans development and execution, CRFs, design and completion, TMF maintenance, protocol amendment and clinical report preparation, as required - Collaborate with Clinical Data Management group to ensure correct CRFs content is collected, prepare comprehensive completion guidelines, and design effective data listings and study reports - Train CROs, vendors, investigators and study coordinators on implementation of study protocol - Hire, train, manage and oversee Clinical trial staff, and
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TITLE: Clinical Lab Operator I
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (unspecified)
SALARY: Not disclosed
POSTED: 2026-06-05
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5775499004
EXCERPT: Clinical Lab Operator I Austin, TX POSITION SUMMARY: Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: • Assist in testing of patient samples according to standard operating procedure. •Meet expected performance metrics within role as applicable. • Responsible for maintaining updated understanding and knowledge of methods performed in the lab • Provide guidance for new team members. • Follows GLP (good laboratory practice): maintain clean and organized workspace • Completes training and other deadlines on time. • Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory's standard operating procedures • Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor • Communicates with team and other departments on various platforms (including via e-mail) • Provides feedback on day-to-day schedule and tasks to lead/supervisor • Assists teammates in completing daily tasks • Maintains equipment and instruments in good operating condition (such as calibration and expiration date) • Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties. • Participate in Continuous Improvement Projects (TAG, 5S) • Conducts himself/herself in a professional manner • Adheres to Departmental Expectations • This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job • Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later
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TITLE: Director, Forward Deployed AI Engineering
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $187K-$233K
POSTED: 2026-05-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5991157004
EXCERPT: Director, Forward Deployed AI Engineering US Remote About the Role The Head of AI Solutions will lead a Forward Deployed AI engineering team and owns the delivery of AI-powered workflow transformation across Sales & Marketing, Finance, Legal, HR, Business Development, Business Operations and other related G&A functions. This is a player-coach role in the truest sense: you lead a team of Forward Deployed AI Solutions Engineers, but you are also consistently in the work alongside them - scoping workflows, building, debugging, and iterating in production. We believe the pace of change in AI makes proximity to the work non-negotiable at every level of the organization. The expectation is that roughly half your time is spent building and shipping alongside your engineers, using that firsthand knowledge to make better prioritization calls, give feedback, and earn the trust of both your team and the business stakeholders you serve. You partner closely with the AI Platform team to ensure every workflow transitions cleanly to long-term ownership, and you bring patterns and reusable assets back to the broader AI & Automation organization. What You'll Own Build and ship alongside your team - Spend meaningful time as a hands-on contributor - scoping workflows end-to-end, building agents and automation pipelines, debugging integration issues, and tuning prompts and context in production. - Set the technical bar through your own work: production-grade evals, observability, clean handoff documentation, and rigorous testing before anything ships. - Jump in when a deployment is stalled, a system integration is unexpectedly gnarly, or
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TITLE: Manager, Clinical Lab
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: $123K-$180K
POSTED: 2026-05-20
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5997398004
EXCERPT: Manager, Clinical Lab San Carlos, CA POSITION SUMMARY Works closely with Senior Manager to ensure company, department, and team goals are met. PRIMARY RESPONSIBILITIES - Monitors workflow and ensures production goals and deadlines are met (e.g. TAT, SLA) - Engages in future planning and scales employees and equipment appropriately - Gathers and monitors metrics on production deadlines, efficiency, scrap waste, and error rates - Monitors the quality control/assurance programs, test results, and equipment (if applicable) - Uses metrics in decision-making and to drive changes across the team (e.g. cost reduction, quality improvement) - Manages sufficient headcount levels to meet production goals by proactively driving the interview process and managing employee PTO and overtime when necessary. - Refines current lab process through continuous improvement projects. - Oversees team specific lab operation. - Go-to person when senior manager is not present; go-to person for knowledge of process and product. - Responsible for seamless transition of automation and test improvement/additions into production workflow - Analyzes and troubleshoots lab processing errors; provides recommendations on how to proceed to lab director, scientists and statisticians as necessary - Supports Supervisors in close out of NCRs. - Responsible for the initiation and close out of CAPAs in a timely manner. - Ensures departmental lab compliance for regulatory bodies - Ensures tests are being completed according to approved procedures. - Maintains an organized, safe and efficient work area for the team at all times. - Actively interacts with interdepartmental teams such as OPS, Accessioning, Engineering, Stats, R&D, and
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TITLE: Clinical Lab Operator I - Temp
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (onsite)
SALARY: Not disclosed
POSTED: 2026-06-02
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5997402004
EXCERPT: Clinical Lab Operator I - Temp Austin, TX POSITION SUMMARY : This is a temporary position scheduled for 6-12 months, located on site in Austin, TX. Available Shift Schedule: Swing Shift: Fri-Tues, 2 pm - 10:30 pm (with 10% shift differential). Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: • Assist in testing of patient samples according to standard operating procedure. •Meet expected performance metrics within role as applicable. • Responsible for maintaining updated understanding and knowledge of methods performed in the lab • Provide guidance for new team members. • Follows GLP (good laboratory practice): maintain clean and organized workspace • Completes training and other deadlines on time. • Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory's standard operating procedures • Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor • Communicates with team and other departments on various platforms (including via e-mail) • Provides feedback on day-to-day schedule and tasks to lead/supervisor • Assists teammates in completing daily tasks • Maintains equipment and instruments in good operating condition (such as calibration and expiration date) • Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties. • Participate in Continuous Improvement Projects (TAG, 5S) • Conducts himself/herself in a professional manner • Adheres to Departmental Expectations • This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper
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TITLE: Associate CQV Engineer
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: Not disclosed
POSTED: 2026-04-06
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5842341004
EXCERPT: Associate CQV Engineer San Carlos, CA Position Summary The Assoicate CQV Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. This is a contract position for three months. Primary Responsibilities: - Work with other Instrument Support Engineers, and the Automation and laboratory teams to respond to instrument failures and ensure proper instrument function. - Diagnose and troubleshoot any system concerns to minimize downtime. - Install new laboratory equipment (e.g., liquid handlers, sequencers, plate sealers, etc.). - Coordinate and/or perform instrument installations and qualifications per equipment protocols. - Work with Quality Assurance to determine qualification (IQ/OQ/PQ), calibration and preventive maintenance requirements for new incoming instruments, as needed, to comply with regulations. - Maintain program for preventative maintenance (PM), routine maintenance, and calibration of all laboratory equipment. - Perform troubleshooting activities and provide Level 1 service; coordinate with Level II's and vendors to address escalated service concerns. - Recommend and implement changes to ensure ongoing high-quality performance of laboratory equipment. - Perform all service activities in compliance with all relevant safety and regulatory bodies (e.g., OSHA, CAP, CLIA, etc.). - Maintain and continuously develop knowledge and expertise related to the
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TITLE: Floater Phlebotomist - Fairfax, VA - Temp
EMPLOYER: Natera, Inc.
LOCATION: Fairfax, VA (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-21
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6001684004
EXCERPT: Floater Phlebotomist - Fairfax, VA - Temp Fairfax, VA Position Summary - Temporary Position location in Fairfax, VA The Floater Phlebotomist/Data Entry Analyst is a dual-role position responsible for providing phlebotomy services across multiple IOPs and performing accurate and timely data entry to support clinical and administrative operations. This role requires excellent organizational skills, attention to detail, the ability to adapt to changing environments and the ability to adhere to a strict schedule. Key Responsibilities Phlebotomy : - Perform blood draws and other specimen collections following standard procedures and protocols. - Ensure the comfort and safety of patients during specimen collection. - Accurately label, document, and process specimens for transport to laboratories. - Maintain compliance with all health and safety regulations, including infection control. - Travel between assigned locations to provide phlebotomy services as needed. - Maintain a clean, organized and fully stocked phlebotomy workspace. Data Entry and Analysis: - Enter patient, specimen, and test information into laboratory information systems (LS) with high accuracy. - Receive, review and enter patient data into laboratory information systems (LIS) with high accuracy. - Review and verify data to ensure completeness and correctness. - Compile, organize, and analyze data for reporting purposes. - Identify and correct data discrepancies or escalate issues a necessary. - Maintain confidentiality and security of patient and organizational data in accordance with HIPAA and other regulations. - Complete data entry in a scheduled, timely manner. - Collaborate with management and internal teams to implement and evaluate improvements. - Understand and
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TITLE: Sr. Commissions Analyst
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-02
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6010462004
EXCERPT: Sr. Commissions Analyst US Remote POSITION SUMMARY: The Senior Commissions Analyst, Sales is responsible for ensuring the timely and accurate calculation of commissions in Xactly. Support the Sales organization by providing timely, accurate, and insightful business expense performance analyses to management. Gathers analyzes, prepares, and summarizes recommendations for financial plans, future requirements, and operating forecasts. PRIMARY RESPONSIBILITIES: - Configuring and managing new compensation plan implementations and changes on Xactly. Handle administrative operations including employee set-up, access management, maintaining hierarchies, and streamlining workflows. - Responsible for all aspects of day to day commission administration in Xactly Incent resulting in accurate and timely commission payments to meet Payroll deadlines. - Troubleshoot and resolve data discrepancies or exceptions within Xactly Incent and effectively communicate outcomes. Submit final payments to payroll and 3rd party vendors to meet payroll deadlines - Preparation of commission approval documents, detailed backup, and conducting commission approval meetings for SOX compliance. - Provide monthly accruals for sales commission and partner with Accounting team ensure these are appropriately are booked Work with sales management to develop monthly forecasts and annual budgets on sales expenses. - Provide monthly accruals for sales commission and partner with Accounting team ensure these are appropriately are booked - This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) to perform the job. - Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training, and security
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TITLE: Corporate Compliance Director
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $160K-$210K
POSTED: 2026-03-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5823888004
EXCERPT: Corporate Compliance Director US Remote POSITION SUMMARY The Director, Corporate Compliance is an individual contributor role that reports to the Sr. Director of Corporate Compliance and assists in leading projects that support overall Compliance initiatives as designated by the Chief Compliance Officer. The position supports the day-to-day functions of the Compliance department as well as special projects and assessments through data analysis, process improvement, auditing, report development, and policy maintenance. PRIMARY RESPONSIBILITIES - Supports the compliance function by developing and executing high level strategic business objectives that support the growth of key business areas. - Supports the compliance department with execution on key strategic objectives of the business that support both long term and short term goals of the three key business units of the company. - Implements key objectives of the Compliance Department that allows for proactive compliance risk identification. - Develops clear, qualitative and/or quantitative analyses in support of Corporate Compliance programs and initiatives. - Develops innovative, interactive, and informative training on a variety of compliance and privacy topics. - Develops, implements, and monitors key compliance functions and risk areas under direction of Sr. Director of Compliance and the Chief Compliance Officer in accordance with OIG guidance for clinical laboratory compliance programs. - Provides analysis and summary reports on an “ad-hoc”, as well as routine basis at the direction of the Sr. Director of Compliance or the Chief Compliance Officer. - Responsible for maintenance of peripheral databases and trackers that support Corporate Compliance reporting needs. - Supports monitoring
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TITLE: Senior Network Engineer
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: $160K-$221K
POSTED: 2026-03-26
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5838334004
EXCERPT: Senior Network Engineer San Carlos, CA POSITION SUMMARY: The Senior Network Engineer supports the design, testing, implementing and monitoring of enterprise Network infrastructure/Operations. This role is an individual-contributor, enterprise-wide role that works closely with and advises other IT and engineering teams on design, deployment, support and monitoring of network systems. The Senior Network Engineer will be the leader for network architecture, design, implementation and operation. PRIMARY RESPONSIBILITIES: - Provide technical inputs and evaluate new and emerging network technologies addressing the gaps identified. - Leads all aspects of network routing & switching design, architecture and equipment lifecycle. - Design and implement network improvements to improve network performance, capacity and scalability. - Leads the performance of day-to-day networking tasks to ensure network reliability, availability and serviceability with minimal interruption. - Provides technical support, responds to work orders and tickets from the users, analyzes and solves reported network problems. - Installing and configuring networking hardware, LAN switches, wifi and firewalls. - Developing and maintaining network architecture drawings and documentation. - Support network compliance and risk management activities. - Review network monitoring tools and respond to alerts. - Part of the team responding to network incidents. - Lead RCA analysis and publish RCA reports as appropriate. - Perform network vulnerability assessments to identify weaknesses and countermeasures; provide timely assessment reports to key stakeholders. - Update network equipment to latest firmware releases. - A member of the 24/7 network operational support team. - This role works with PHI on a regular basis both in paper
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TITLE: Manager of Clinical Trials Budgets and Contracts
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $130K-$160K
POSTED: 2026-02-03
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5780448004
EXCERPT: Manager of Clinical Trials Budgets and Contracts US Remote OVERVIEW: As a member of the Budget, Contracts and Payments (BCP) team, the Manager of Clinical Trials Budgets & Contracts is responsible for oversight of clinical agreements, budgets, payment follow up and corresponding processes. The Manager of Budgets & Contracts oversees the execution of high‐quality clinical agreements and budgets in a timely manner that balances the needs of all parties while maintaining internal and external relationships. This role is responsible for a team of Budget & Contract Managers and Analysts, who will report directly into them. This individual will work closely with clinical study leads, legal, accounts payable, finance, other cross-functional partners, clinical site personnel and external stakeholders to lead improvement initiatives, manage vendor relationships, contract execution, and site budgets, and ensure site payment reconciliations. This role reports into the the Associate Director of Clinical Trial Business Operations All clinical agreement work will be done in accordance with company policies, Standard Operating Procedures (SOPs), legal and regulatory requirements, and using fair market valuation. PRIMARY RESPONSIBILITIES: - Propose and implement solutions for identified gaps in budget, contract, and payment reconciliation processes. - Partner closely with legal and accounts payable to implement cross-functional process improvements. - Manage full time and/or contracted Budget & Contract Managers (BCM). - Manage full time and/or contracted Budget & Contract Analysts (BCA). - Ensure that budgets processed by their team are loaded into systems such as CTMS for payment. - Responsible for the day‐to‐day management of assigning and
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TITLE: Oncology Pathology Assist - 2nd Shift
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-04-15
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5967961004
EXCERPT: Oncology Pathology Assist - 2nd Shift US Remote POSITION SUMMARY: This position supports our 2nd Shift operations, with a scheduled start time of 12:00 PM PST. The Oncology Pathology Assistant (Histology Technologist) provides assistance to the Signatera team as a subject matter expert for review of clinical pathology reports. The Histology technologist will assist the medical and customer service teams with acquisition of appropriate specimens for minimal residual disease (MRD) testing in oncology. PRIMARY RESPONSIBILITIES: - Assist the medical and customer service teams with the interpretation of oncology pathology reports to identify optimal samples to request when initial FFPE blocks or slides are inadequate for testing. - Read and ensure accurate curation of clinical history, diagnosis, progress notes, and specimen information is entered into the Signatera sample database. - Assist with devising strategies to stratify data for retrieval from the Signatera sample database and other databases as necessary. - Maintain proficiency with and help organize diagnostic data according to pertinent WHO guidelines. - Serve as subject matter expert to the Laboratory Director, Genetic Counseling, Customer Experience, Sales, and Clinical Trial teams for pathology reports. - Assist in the identification and alert the Laboratory Director when samples may have been collected at suboptimal timepoints and/or fixative conditions. - Assist Genetic Counseling and Customer Experience teams in identification and procurement of optimal additional samples, as necessary. - Provide professional support for the Clinical Trial team through accurate and organized data transfer. - Performs other duties as assigned. QUALIFICATIONS: - Bachelor's degree, or
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TITLE: Forward Deployed AI Solutions Engineer
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $113K-$172K
POSTED: 2026-01-23
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5766365004
EXCERPT: Forward Deployed AI Solutions Engineer US Remote About the role The Forward Deployed Solutions Engineer will work directly within a business domain (e.g., Commercial, Clinical Operations, Lab Operations, Sales & Marketing, Customer Experience etc.). In your role, you'll find opportunities for enhancing efficiency and productivity by looking for workflows which can be executed 10-100x faster or more often than a human team could using AI agents, integrations and other patterns. You will build, deploy, and run them in production. You report into the central AI & Automation team, partner directly with domain leadership on priorities, and bring patterns back so the whole company compounds. Find the leverage in your domain - Map the workflows in your domain - the ones running today, and the ones that don't exist yet because they weren't feasible without agents or automation tools. - Identify the step-change opportunities: where AI, ML, or automation unlock throughput, coverage, or speed. - Build the business case, quantify projected impact, and align with domain leadership on priorities. Design the future-state workflow - Map structured and unstructured data flows across the systems involved (CRM, ERP, ticketing, document stores, internal tools, external SaaS). - Define the target workflow: what the agent does, what the human does, and where they hand off. - Figure out what context the agent or model needs to do the work well - and how to get it there reliably (retrieval, grounding, tool access, memory). - Design human-in-the-loop checkpoints so review adds value without becoming the bottleneck.
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TITLE: Lead Clinical Lab Scientist
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: Not disclosed
POSTED: 2026-04-10
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5837420004
EXCERPT: Lead Clinical Lab Scientist San Carlos, CA POSITION SUMMARY: Assists in analyzing specimens and works closely with supervisor to make sure production goals are met. PRIMARY RESPONSIBILITIES: - Verify the proper specimen being analyzed for patients and perform correct tests that need to be completed - Assists the team in day-to-day lab work according to standard operating procedure with little to no errors - Follows GLP (good laboratory practice); reports non-conformity of SOPs to supervisor/manager - Ensures production work is consistently completed in a timely manner. - Ensures all case samples are processed and accounted for - Assists supervisor in completing side projects assigned by the manager - Go to person on the lab floor and when supervisor is not present - Trains new hires with the current lab processes and assists supervisor in training/implementation of new process changes. - Assists supervisor and lab trainer in completing competency for staff. - Train on specialized instructions for instruments/protocols (super users) - Recognizes and escalates equipment malfunctions; troubleshoots most errors - Understands the entire lab process and identifies/troubleshoots issues when they arise. - Ensures new lab changes are implemented properly on the lab floor - Escalates lab issues and team concerns to supervisor and/or manager. Suggests possible solutions. - Escalates any discrepancies of team members' performance to supervisor - Provides feedback during performance evaluations for team members - Meets regularly with the Supervisor - Keeps team morale up and maintains professionalism of team members, including by acting as a role model -
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TITLE: Research Associate 1
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-27
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6004657004
EXCERPT: Research Associate 1 Austin, TX POSITION DURATION: Six-month contract role with potential to extend or convert to FTE based on performance and business needs POSITION SUMMARY: We are seeking a highly motivated and skilled Research Associate I to join our dynamic team in the sample management. In this role, you will be responsible for the management of biological samples, ensuring their integrity, overseeing quality control, and supporting research projects that rely on biological specimens. The ideal candidate will have a strong background in bio sample management, research methodologies, and data analysis, with an interest in contributing to cutting-edge scientific research. PRIMARY RESPONSIBILITIES: - Sample Collection and Processing : - Oversee the collection, preparation, and processing of biological samples (e.g., blood, tissue, saliva, DNA) in accordance with established protocols and best practices - Maintain proper documentation and labeling of samples, ensuring traceability from collection to storage - Sample Storage and Management : - Ensure proper storage conditions (e.g., temperature, humidity) for various types of biological samples, including cryopreservation and ambient storage - Implement inventory management procedures to track and organize samples, utilizing database systems and laboratory management software (e.g., FreezerPro, LabArchives) - Ensure the samples are appropriately cataloged and accessible to researchers in a timely manner - Database Management and Data Analysis : - Manage and update the sample database, ensuring accuracy and compliance with sample tracking and research needs - Assist in data analysis and reporting, including the creation of sample inventory reports and performance metrics - Collaborate with the
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TITLE: Supervisor Clinical Lab
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: $107K-$161K
POSTED: 2026-03-20
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5828560004
EXCERPT: Supervisor Clinical Lab San Carlos, CA Position Summary The Supervisor of the clinical laboratory is a member of the Operations Department whose role is to oversee employees' performance and serve as a liaison between employees and senior management to meet company goals and quality objectives. The supervisor is responsible for daily supervision of lab staff performing duties such as laboratory testing and data review. Duties include but are not limited to coaching, motivating, staffing, evaluating, and training staff. The supervisor works closely with the manager to ensure company and team goals are met while adhering to good manufacturing practices and CLIA/CAP guidelines. The shift timings are from 3.00 PM- 1.30 AM PRIMARY RESPONSIBILITIES - Provides direct supervision to professional individual contributors and/or skilled, support individual contributors - Ensures production work is consistently completed according to department goals. - Administers company policies that directly affect subordinate employees. - Monitors team members to ensure adherence to SOPs and safety procedures - Oversees training and development of all staff members - Document nonconformances and all corrective actions taken when test systems deviate from the established performance specifications as needed. Escalates protocol deviation to lead/supervisor. - Handles employee issues in collaboration with the department manager and Human Resources. - Ensures alignment with team for reasoning behind instructions/processes and changes - Plans and leads shift meetings. Meets regularly with individual team members to discuss goals and progress - Go-to person when manager is not present. - May assist lab team in day-to-day tasks - Keeps
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TITLE: Bilingual International Customer Support Representative
EMPLOYER: Natera
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-05
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5995577004
EXCERPT: Bilingual International Customer Support Representative US Remote POSITION SUMMARY The International Customer Support Representative provides world-class service to our international customers. This position will serve as the primary point of contact for our international Sales team and international customers. This role will assist healthcare professionals, laboratories, and other internal and external partners to ensure a smooth ordering and reporting process, ensuring a smooth experience throughout the entire customer journey. The ideal candidate will be passionate about providing excellent support and a willingness to quickly learn about our products and services. This role requires the ability to work independently, multi-task, and use critical thinking skills to troubleshoot and resolve issues in a timely manner. PRIMARY RESPONSIBILITIES - Provide timely and accurate information to international customers and internal teams via phone, email, and other electronic channels - Manage high volume of international customer accounts and their support needs - Resolve customer inquiries and issues promptly and communicate the resolution clearly and logically. Troubleshoot the issue and identify the root cause - Partner with Sales team counterparts to follow-up on missing information needed to process and report ordered tests - Document all customer interactions, communications, actions taken, and follow ups in our customer service applications - Collaborate with internal teams such as sales, product development, and lab operations to ensure customer needs are met effectively - Coordinate with logistics and shipping teams to resolve any shipping, customs, or delivery issues related to kits or samples - Provide training and educational support to our
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TITLE: Sr Phlebotomist - Jersey City, NY
EMPLOYER: Natera, Inc.
LOCATION: Jersey City, NY (remote)
SALARY: Not disclosed
POSTED: 2026-05-08
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5991894004
EXCERPT: Sr Phlebotomist - Jersey City, NY Jersey City, NY *THIS IS NOT A REMOTE POSITION. THIS IS AN IOP IN JERSEY CITY, NY* POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to
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TITLE: Clinical Biospecimen Operations Associate
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (unspecified)
SALARY: $88K-$110K
POSTED: 2026-06-11
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6020418004
EXCERPT: Clinical Biospecimen Operations Associate Austin, TX POSITION SUMMARY: The Clinical Biospecimen Operations Associate executes oncology clinical research studies, including coordination of all operational activities required for tracking, testing and reporting clinical trial samples. This position will perform required job duties with oversight from the Pharma Operations Team Leader and will work closely with internal and external central testing laboratories, vendors, Data Management, Product Management, Engineering and external collaborators in compliance with the study protocol(s), SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES: - Maintain oversight of all study sample operational activities including planning, coordinating and tracking clinical trial sample testing to ensure results are provided within agreed upon TAT - Work with Data Management to develop and maintain dashboards and KPIs representing metrics and trends related clinical trial sample testing and the status of clinical studies and present to study teams and management teams, as needed. - Meticulously track clinical trial samples from sample receipt to result reporting to investigator sites and/or external collaborators (and sample return, if applicable) - Utilize operational and project management skills to anticipate, investigate and resolve issues to ensure deliverables and TAT are met; raise issues to Pharma Operations Team Leader - Responsible for handling data files to support timely result reporting - Review and provide input to clinical study protocol for sample collection requirements and alignment with the SOW, study plans and company policies - Administer clinical trial supplies related to biospecimen collection, processing, shipment, and storage as, well as maintenance of associated tracking information
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TITLE: Lead AI Architect, Salesforce Service Cloud & AWS
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (unspecified)
SALARY: $153K-$191K
POSTED: 2026-02-06
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5795477004
EXCERPT: Lead AI Architect, Salesforce Service Cloud & AWS Austin, TX POSITION SUMMARY We are seeking a visionary Lead AI Architect to lead the design and implementation of next-generation AI solutions by bridging our Salesforce CRM ecosystem with AWS cloud infrastructure. In this strategic role, you will be responsible for architecting scalable Generative AI applications that enhance customer engagement, automate complex workflows, and unlock predictive insights. You will serve as the technical authority on how Salesforce Data Cloud, Einstein Trust Layer, and Amazon Bedrock interact, ensuring our AI solutions are secure, scalable, and impactful. You will move beyond simple integrations to build robust "Bring Your Own Model" (BYOM) architectures. PRIMARY RESPONSIBILITIES AI Strategy & Architecture (40%) - Define the end-to-end architecture for Generative AI solutions, integrating Salesforce Data Cloud with Amazon Bedrock and SageMaker . - Design "Bring Your Own Model" (BYOM) patterns, allowing Salesforce to securely access Foundational Models (FMs) hosted on AWS (e.g., Claude, Titan, Llama 2) via Bedrock. - Architect the data ingestion and grounding strategies (RAG - Retrieval Augmented Generation) to ensure AI models have access to real-time, unified customer profiles from Data Cloud. - Establish the governance framework for AI, ensuring compliance with the Einstein Trust Layer regarding data privacy, zero-data retention policies, and PII masking. Implementation & Development (30%) - Lead the technical implementation of Model Builder and Prompt Builder within Salesforce, connecting them to external AWS endpoints. - Configure Amazon Bedrock agents and knowledge bases to execute complex tasks and retrieve proprietary data for
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TITLE: Sr Phlebotomist - Schertz, TX
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-14
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5995908004
EXCERPT: Sr Phlebotomist - Schertz, TX US Remote POSITION SUMMARY **This position is not remote, it is located in Schertz, TX** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI
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TITLE: Sr Phlebotomist-Bowie, MD
EMPLOYER: Natera, Inc.
LOCATION: Bowie, MD (remote)
SALARY: Not disclosed
POSTED: 2026-05-14
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5995919004
EXCERPT: Sr Phlebotomist-Bowie, MD Bowie, MD POSITION SUMMARY **This position is not remote, it is located in Bowie, MD** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and
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TITLE: Sr Phlebotomist - Smith Glynn, MO
EMPLOYER: Natera, Inc.
LOCATION: Springfield, MO (onsite)
SALARY: Not disclosed
POSTED: 2026-05-14
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5992958004
EXCERPT: Sr Phlebotomist - Smith Glynn, MO Springfield, MO ****This is an onsite position in Smith Glynn, Missouri*** POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper
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TITLE: Sr Phlebotomist - New Orleans, LA
EMPLOYER: Natera, Inc.
LOCATION: New Orleans, LA (onsite)
SALARY: Not disclosed
POSTED: 2026-05-21
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5992966004
EXCERPT: Sr Phlebotomist - New Orleans, LA New Orleans, LA POSITION SUMMARY **This position is located on site in New Orleans, LA** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access
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TITLE: Supervisor, Test Coordinator - Houston, TX
EMPLOYER: Natera, Inc.
LOCATION: Houston, TX (unspecified)
SALARY: Not disclosed
POSTED: 2026-03-02
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5815402004
EXCERPT: Supervisor, Test Coordinator - Houston, TX Houston, TX Test Coordinator Supervisor - Houston, TX Position Summary The Supervisor for the Test Coordination Team will be responsible for leading and supporting a team of Test Coordinators, ensuring excellence in patient care coordination, phlebotomy services, and administrative operations. This role focuses on day-to-day team management, operational efficiency, compliance, and the development of team members. The Supervisor acts as the primary escalation point for internal and external queries, supporting seamless collaboration between field teams, patients, and operational departments. This position requires strong organizational, leadership, and communication skills, and will include up to 50% travel to support audits, onsite visits, and team training initiatives. Primary Responsibilities Team Leadership & Management - Provide daily supervision and support to the Test Coordinator team. - Serve as the first line of escalation for operational issues, patient and account inquiries, and procedural uncertainties. - Conduct biweekly 1:1 meetings with each direct report to promote engagement, identify training needs, and track performance. - Review and approve employee timecards and manage scheduling to align with clinic and organizational requirements. Operational Oversight - Ensure Test Coordinators maintain compliance with specimen handling protocols, EMR documentation, and patient identification practices. - Monitor key metrics and proactively mitigate issues that could impact operational performance. - Oversee supply chain needs, including ordering and tracking supplies for all test coordination activities. Quality Assurance & Audit Support - Assist with the coordination and execution of internal and external audits - Conduct regular quality checks on patient coordination
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TITLE: Sr Phlebotomist - Marrero, LA
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-21
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5992974004
EXCERPT: Sr Phlebotomist - Marrero, LA US Remote POSITION SUMMARY **This position is not remote, it is located in Marrero, LA** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI
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TITLE: Production Planner
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: $84K-$106K
POSTED: 2026-03-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5822234004
EXCERPT: Production Planner San Carlos, CA POSITION LOCATION: The Production Planner creates and maintains headcount, equipment, and facility capacity plans to meet output targets in 24/7 genetic testing labs. This role develops and communicates production schedules, production targets, and continuously monitor performance versus plan. Provides daily/weekly reporting of lab KPIs and schedules to lab leadership and interfaces across the organization, including but not limited to Lab Operations, Process Engineering, Equipment support, Analytics, Product Managers, and Engineering to optimize lab production. PRIMARY RESPONSIBILITIES: - Develop and maintain capacity models for headcount, equipment, facilities across multiple labs.. - Create daily, weekly, and monthly production schedules aligned to production goals. - Monitor shift-level execution against plan, highlight deviations >5% and remedial plans - Partner with Lab Operations leaders realign WIP and production priorities to overcome production constraints. - Track and report KPIs; QCDS, schedule adherence, cycle time, bottleneck queues, OEE. - Partner with Continuous Improvement teams and other individuals on identifying production constraints and improving scheduling for higher throughput and quality. - Analyze data across multiple platforms including (SQL, Qlikview, PowerBI, LIMS, gSuite, JIRA, etc.) to uncover issues/bottlenecks and work with Lab Leaders on driving improvements. - Establishes and manages escalation pathway for delayed or problematic samples in concert with Lab Leaders and internal stakeholders. - Confers with management to resolve problems, roadblocks, and barriers to progress. - Effectively communicates production expectations to team members and stakeholders in a timely and clear fashion - This role works with PHI on a regular basis both
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TITLE: Sr. Technical Product Manager - Data & Applied AI (Patient Experience & Commercial Operations)
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $141K-$176K
POSTED: 2026-04-07
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5850674004
EXCERPT: Sr. Technical Product Manager - Data & Applied AI (Patient Experience & Commercial Operations) US Remote Role Overview We are seeking a Sr. Technical Product Manager to lead the strategy and execution of data product, AI/ML system, AI-powered tooling, and automation initiatives across Patient Experience and Commercial Operations functions. This role is focused on improving how patients navigate testing and billing while enabling operational teams to efficiently progress cases from order to completion. You will play a crucial part in supporting initiatives to reduce friction, improve patient trust, and increase operational efficiency, ultimately driving better conversion, collections, and experience. This role focuses on building, scaling, and leveraging platforms and products that power decision intelligence and activity orchestration across these domains. You will work in close collaboration with domain leaders while building through centralized Data & AI organization platforms, standards, and governance. You will own the full product lifecycle from discovery through production, ensuring solutions are adopted, trusted, and deliver measurable business impact. In doing so, you will work hands-on as an empowered builder of AI and software solutions to improve workflow efficiency, productivity, and quality for the teams you support. This is a technical product role requiring fluency in data systems, modern data platforms, ML, and AI implementation patterns (and the ability and drive to build with them directly), combined with strong experience and stakeholder intuition across the associated functions. The role has direct ownership of high-impact initiatives that deeply influence organizational success. What You'll Do Strategy & Roadmap -
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TITLE: Sr Phlebotomist - Fulton, MD
EMPLOYER: Natera, Inc.
LOCATION: Fulton, MD (remote)
SALARY: Not disclosed
POSTED: 2026-06-02
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6010350004
EXCERPT: Sr Phlebotomist - Fulton, MD Fulton, MD This is NOT a remote position. This position is located in Fulton, MD. A minimum of 5 years of phlebotomy experience is required. ___________________________________________________________________________________________________ POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper
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TITLE: Sr Product Manager
EMPLOYER: Natera, Inc.
LOCATION: Japan (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-12
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5994524004
EXCERPT: Sr Product Manager Japan LOCATION: Tokyo, Japan POSITION SUMMARY: We are seeking a highly motivated and strategic Product Manager to support the commercial launch and ongoing growth of Signatera in Japan. This role will work closely with the U.S.-based Global Product Management organization and the local Japanese commercial team in Japan to execute launch activities, support field readiness, and drive successful adoption of Signatera in Japan. The position sits at the intersection of product management, commercial execution, and cross-functional collaboration, serving as a key liaison between the Japan commercial organization and the U.S.-based parent company. The successful candidate will help translate global product strategy into effective local market execution while providing market insights and feedback to the broader global product management team. The ideal candidate brings a blend of experience across product management, commercialization, and marketing, leveraging next-generation sequencing technologies for oncology diagnostics. PRIMARY RESPONSIBILITIES: - Support the execution of commercial launch activities for Signatera in Japan, including pre-launch planning, launch readiness, and post-launch support - Drive adoption and utilization across markets by partnering closely with Sales and Marketing teams - Assist in identifying and addressing local market needs, operational gaps, and customer experience opportunities - Support implementation and optimization of workflows from ordering through results delivery to enhance customer experience - Partner with the marketing, medical affairs, and Global Product Management teams to support development and localization of sales training content and support field onboarding materials - Develop clear, scalable materials and documentation to communicate workflows effectively to internal
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TITLE: Organ Health Specialist, Abdominal Transplant
EMPLOYER: Natera, Inc.
LOCATION: Seattle, WA (unspecified)
SALARY: $180K-$200K
POSTED: 2026-04-01
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5843326004
EXCERPT: Organ Health Specialist, Abdominal Transplant Seattle, WA Territory: PNW, includes Washington, Oregon and Northern California. Ideal candidate can reside in PNW. We are seeking an experienced Organ Health Specialist (OHS) - Abdominal Transplant to join our growing Organ Health Sales team! In this role, you will drive revenue growth and market development within transplant markets by cultivating and maintaining key relationships, executing strategic business plans, and promoting the adoption of both existing and newly launched products. Your expertise and insights will play a critical role in advancing our mission to support healthcare providers with innovative diagnostic tools. The ideal candidate is a results-driven professional with a proactive mindset, adept at navigating complex sales environments and overcoming challenges. If you're eager to make a lasting impact on transplant patient care while thriving in a fast-paced, competitive sales role, we encourage you to apply. Primary Responsibilities: As an Organ Health Specialist - Abdominal Transplant, you will drive sales and adoption of Prospera , a non-invasive blood test for transplant patients. This role focuses on transplant centers, where the OHS will engage with transplant specialists, and key decision-makers to integrate Prospera into clinical practice. In addition to Prospera you will also promote Renasight , a genetic test that identifies potential genetic causes of kidney disease and assesses hereditary risks. This high-impact, competitive role demands a strategic sales approach, strong client relationships, and deep expertise in the transplant market. - Achieve and exceed sales goals through strategic sales initiatives, relationship-building, and effective territory management.
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TITLE: Sr Phlebotomist-Sterling, VA
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-04-10
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5893917004
EXCERPT: Sr Phlebotomist-Sterling, VA US Remote POSITION SUMMARY - ** This position is not remote, it is located in Sterling, VA** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI
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TITLE: Director, Head of Product Management – AI-Enabled Precision Medicine (Therapeutics & Innovations)
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $185K-$231K
POSTED: 2026-05-15
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5994721004
EXCERPT: Director, Head of Product Management – AI-Enabled Precision Medicine (Therapeutics & Innovations) US Remote Director, Head of Product Management - AI-Enabled Precision Medicine (Therapeutics & Innovations) About Us We are redefining the future of precision medicine by integrating AI with healthcare to create next-generation, precision treatment modalities. Our multidisciplinary team is building products at the intersection of clinical data, multi-omics, and machine learning-unlocking entirely new approaches to drug development and patient care. Within the Therapeutics & Innovations Business Unit, we are developing a new category that bridges diagnostics and therapeutics. Our platform combines deep scientific expertise with proprietary datasets to power AI-enabled solutions that can transform how therapies are discovered, developed, and deployed. We are looking for a product leader who can translate this potential into real, scalable products-owning the strategy, roadmap, and execution to bring these innovations to market. The Role We are seeking a Director / Head of Product Management to lead product strategy and execution for our AI-enabled therapeutics platform. This is a highly cross-functional leadership role at the center of science, engineering, clinical development, and commercial strategy. You will define what we build, why it matters, and how it creates value-for biopharma partners, clinicians, and ultimately patients. You will own the product lifecycle end-to-end: from concept and validation through development, launch, and iteration. This role requires a rare blend of scientific fluency, product rigor, and commercial instinct . You will work closely with R&D, AI, medical, business development, and marketing to ensure our products are scientifically
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TITLE: Rare Disease Specialist (National)
EMPLOYER: Natera, Inc.
LOCATION: United States (unspecified)
SALARY: $200K-$250K
POSTED: 2026-03-09
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5803077004
EXCERPT: Rare Disease Specialist (National) United States POSITION SUMMARY We are seeking experienced clinical sales leaders with five or more years of proven success in diagnostics or specialty laboratory services to join our Rare Disease team. The Rare Disease Specialist (RDS) will be both a frontline sales driver and a strategic business partner, leading market expansion and shaping how we launch and grow our exome and genome testing portfolio across the U.S. As a Rare Disease Specialist, you will focus on engaging key clinical stakeholders, including developmental pediatricians, pediatric neurologists, genetic counselors, and medical geneticists, to drive awareness and adoption of our exome and genome testing solutions. This role is designed for high performers who excel at complex clinical sales, thrive in entrepreneurial environments, and want to leave a lasting mark on the rare disease landscape. PRIMARY RESPONSIBILITIES - Own revenue growth and market development by driving direct sales to developmental pediatricians, pediatric neurologists, genetic counselors, and medical geneticists. - Lead new product launches and accelerate the adoption of clinical exome and genome testing solutions. - Build and sustain high-value relationships across Children's Hospitals, rare disease networks, and clinical decision-makers. - Design and execute territory business plans, with a clear focus on revenue acceleration and market share capture. - Drive proposal development, pricing strategy, and contract negotiations to secure new business and formalize partnerships. - Engage executive leadership with pipeline insights, opportunity prioritization, and performance metrics tied to rare disease growth. Serve as a clinical and technical resource, delivering education and
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TITLE: Mgr, Inside Sales-Central Timezone
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $84K-$106K
POSTED: 2026-05-27
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6004722004
EXCERPT: Mgr, Inside Sales-Central Timezone US Remote POSITION SUMMARY: The Inside Sales Manager is a senior level commercial position responsible for strategically leading the Inside Sales Team. As the team leader, the Inside Sales Manager is accountable to develop inside sales strategies and tactics to support the outside sales team and grow our customer base. The team assesses and handles inbound lead calls, makes outbound sales and customer retention calls, and gathers critical sales opportunity information to pass to the field sales team. Working closely with field sales management colleagues, the Inside Sales Manager leading the Inside Sales Representatives, will develop and implement action plans to increase the customer base, maximize sales revenue and increase market share by demonstrating commitment to surpass our customers' expectations. PRIMARY RESPONSIBILITIES: - Oversee daily activities performed by the Inside Sales Team and support all escalations, driving each member toward expected weekly, monthly and quarterly goals through regular coaching and 1:1's. - Collaborate with Marketing and Sales teams to develop and execute on quarterly call campaigns. - Coordinates budgets, organizing and implementing sales strategies, and is responsible for achieving overall sales objectives. - In conjunction with marketing and sales management, develop new product scripts and advanced qualifying questions for call campaigns. - Maintain and develop Inside Sales processes, lead generation, and quarterly project planning, to establish an approach for successful solution selling. - Develop and publish weekly/monthly performance dashboard reports for each Inside Sales Representative utilizing data captured through CRM module activity details and call metrics.
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TITLE: Sr Phlebotomist -Las Vegas, NV (Southern Hills)
EMPLOYER: Natera, Inc.
LOCATION: Las Vegas, NV (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-21
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6001996004
EXCERPT: Sr Phlebotomist -Las Vegas, NV (Southern Hills) Las Vegas, NV POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the
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TITLE: Sr Phlebotomist-Hickory NC
EMPLOYER: Natera, Inc.
LOCATION: Hickory, NC (remote)
SALARY: Not disclosed
POSTED: 2026-04-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5921601004
EXCERPT: Sr Phlebotomist-Hickory NC Hickory, NC POSITION SUMMARY **This position is not remote, it is located in Hickory NC* * A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper
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TITLE: Sr Phlebotomist - Fairfax, VA
EMPLOYER: Natera, Inc.
LOCATION: Fairfax, VA (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-21
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6001841004
EXCERPT: Sr Phlebotomist - Fairfax, VA Fairfax, VA POSITION SUMMARY - **This position is located in Fairfax, VA** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic)
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TITLE: Sr Phlebotomist - Hazelwood, MO
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-14
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5992970004
EXCERPT: Sr Phlebotomist - Hazelwood, MO US Remote ****This is an onsite position in Hazelwood, Missouri**** POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic)
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TITLE: Sr Phlebotomist - Gretna, LA
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-11
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5992972004
EXCERPT: Sr Phlebotomist - Gretna, LA US Remote POSITION SUMMARY **This position is not remote, it is located in Gretna, LA* A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI
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TITLE: Sr Phlebotomist - Fort Smith, Arkansas
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-09
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6015897004
EXCERPT: Sr Phlebotomist - Fort Smith, Arkansas US Remote ****This is an onsite position in Fort Smith, Arkansas**** POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper
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TITLE: Sr Phlebotomist - Livonia, MI
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-04-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5893901004
EXCERPT: Sr Phlebotomist - Livonia, MI US Remote ****This is NOT a remote position, it will be onsite Monday - Friday in Livonia, MI *** POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access
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TITLE: Sr Phlebotomist - St. Louis, Missouri
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-11
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5993327004
EXCERPT: Sr Phlebotomist - St. Louis, Missouri US Remote ****This is an onsite position in St. Louis, Missouri**** POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper
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TITLE: Sr Phlebotomist-El Paso, Texas
EMPLOYER: Natera, Inc.
LOCATION: El Paso, TX (unspecified)
SALARY: Not disclosed
POSTED: 2026-06-10
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6018643004
EXCERPT: Sr Phlebotomist-El Paso, Texas El Paso, TX POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job - Employee
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TITLE: Sr Phlebotomist- Methuen, MA
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-04-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5893905004
EXCERPT: Sr Phlebotomist- Methuen, MA US Remote ***This position is an onsite position located in Methuen, MA **** POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper
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TITLE: Rev Cycle Medical Records Case Mgr-Temp
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-28
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5970012004
EXCERPT: Rev Cycle Medical Records Case Mgr-Temp US Remote Job Description Summary The Revenue Cycle Medical Records Case Manager will support documentation of medical necessity by facilitating medical records (MR) collection and client outreach, by offering expert review and interpretation on a case by case basis, and by maintaining collaborative and productive relationships within the organization relating to Revenue Cycle Management. Job Responsibilities: - Successfully obtain necessary medical documentation by collaborating with and serving as a primary liaison between in-house billing operations, customer experience groups and clinic medical records departments - Have a thorough understanding and knowledge of applicable CMS, state, and insurer medical policy and coverage guidelines (in particular LCD & NCD Coverage Criteria) - Ability to navigate and extract data from multiple versions of electronic medical records, including EPIC - Serve as a source of knowledge for medical records (MR) review and interpretation, including in-depth review of provider progress notes and charts with the ability to identify critical data points highlighting why patient criteria meets medical necessity and summarizing in a succinct manner for health insurance companies - An in-depth knowledge and understanding of oncology and organ health terminology (including chemotherapy treatments and well as immunotherapy treatments) - Develop and cultivate ongoing working relationships with other departments impacting revenue cycle performance - Participate in weekly meetings, daily discussions, case reviews and continuing education to review key metrics, workflows, trends, and performance improvement opportunities - Prioritize performance initiatives and ensure productivity goals are achieved within a timely manner while maintaining
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TITLE: Principal, Pharmacovigilance / Device Vigilance
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $161K-$201K
POSTED: 2026-05-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5993187004
EXCERPT: Principal, Pharmacovigilance / Device Vigilance US Remote POSITION SUMMARY: The Principal, Pharmacovigilance / Device Vigilance is a detail-oriented and proactive professional supporting the safety surveillance of In Vitro Diagnostic and Software-driven products across their lifecycle, including clinical studies and post-market activities. This role is responsible for the collection, assessment, reporting, and management of adverse events, product complaints, and safety data for both medicinal products and medical devices, ensuring compliance with global regulatory requirements. The position plays a critical role in ensuring compliance with global regulatory requirements (e.g., FDA, EU IVDR, Japan) and maintaining the highest standards of patient safety and product quality across both laboratory-developed tests and regulated IVD products, including software/algorithm-based components. PRIMARY RESPONSIBILITIES: - Pharmacovigilance (Drug Safety) - Perform case intake, triage, and processing of Individual Case Safety Reports (ICSRs) - Process and evaluate adverse events associated with diagnostic use (e.g., clinical impact of false positives/negatives) - Coordinate medical review and causality assessment of adverse events - Coordinate timely submission of safety reports (e.g., MedWatch, EudraVigilance, CIOMS) - Support aggregate reporting (PSUR/PBRER, DSUR, annual reports) - Maintain and ensure compliance with global PV regulations (FDA, EMA, ICH, etc.) - Contribute to signal detection and risk management activities - IVD Device Vigilance - Review, triage, and assess product complaints and adverse events related to genetic and diagnostic testing, including incorrect, delayed, or misinterpreted results - Evaluate reportability of events under FDA (MDR), EU IVDR vigilance, Japan and other global regulations - Prepare and submit Medical Device Reports (MDRs) and
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TITLE: Sr Phlebotomist - Little Elm/Frisco, TX
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-11
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5993331004
EXCERPT: Sr Phlebotomist - Little Elm/Frisco, TX US Remote POSITION SUMMARY **This position is not remote, it is located in Little Elm/Frisco, TX** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to
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TITLE: Staff Scientist, R&D (Women's Health)
EMPLOYER: Natera, Inc.
LOCATION: San Carlos, CA (unspecified)
SALARY: $157K-$197K
POSTED: 2026-05-26
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6001235004
EXCERPT: Staff Scientist, R&D (Women's Health) San Carlos, CA We are looking for an inquisitive and creative Staff Scientist to initiate, direct, and execute pre-product scientific research with an emphasis in Women's Health. This Staff Scientist will investigate the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problem solving. The ideal candidate will have broad knowledge of state-of-the-art molecular biology principles, with hands-on experience in next-generation DNA/RNA sequencing, nucleic acid technologies, multiomics, molecular diagnostics development, and/or proteomics. PRIMARY RESPONSIBILITIES: - Contributes substantially and intellectually to research and development - Independently leads projects to create and develop novel nucleic acid based diagnostic tests; including planning, feasibility testing, protocol development, and optimization - Responsible for executing projects as per associated timelines and deliverables - Thoroughly comprehends the objectives and vision of the work - Develops plans, generates and advances new ideas - Performs basic data analysis, including statistics - Independently designs and executes moderate to high complexity experiments - Coordinates the execution and analysis of effective experiments with statistics and bioinformatics teams - Ability to work cross-functionally with statistics, bioinformatics, product development, and project management teams - Documents research progress under a Quality Management System - May manage Research Associates - May work with partners and outside collaborators - Communicates progress directly with colleagues and senior management QUALIFICATIONS: - Ph.D. in molecular biology or closely related field - Minimum of 8 years of industry experience or 2 years of post-doctoral research + 6 years of
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TITLE: Sr Phlebotomist - Rockville, MD
EMPLOYER: Natera, Inc.
LOCATION: Rockville, MD (unspecified)
SALARY: Not disclosed
POSTED: 2026-05-21
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6001994004
EXCERPT: Sr Phlebotomist - Rockville, MD Rockville, MD POSITION SUMMARY A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job - Employee
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TITLE: Sr Phlebotomist - Waco, TX
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-02
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6010346004
EXCERPT: Sr Phlebotomist - Waco, TX US Remote POSITION SUMMARY **This position is not remote, it is located in Waco, TX** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI
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TITLE: Pathology Support Coordinator - Sample Review- (ASCP Certified)- TEMP Position Tues-Saturday (2nd Shift)
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-08
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5838834004
EXCERPT: Pathology Support Coordinator - Sample Review- (ASCP Certified)- TEMP Position Tues-Saturday (2nd Shift) US Remote PRIMARY RESPONSIBILITIES: Leverage multiple information sources, including LIMS, to review cases for accuracy and completeness of pathology tissue samples for Signatera and Altera testing. Interpret pathology reports, clinical notes and additional testing reports to complete light data entry for each tissue sample. Collaborate with team members to work to resolve potential discrepancies. Ensure that necessary notes and holds are placed on cases for non-conforming samples, discrepancies and/or missing information and escalated to ensure timely resolution. Confirm cancer types for the reporting team before the report is issued via emails and spreadsheet. Meet daily case metrics. Attend interdepartmental meetings. Provide feedback on the current process or workflow. Review and understand all SOPs. This role works with PHI on a regular basis both in paper and electronic form and has access to various technologies to access PHI (paper and electronic) in order to perform the job Employee must complete training relating to HIPAA/PHI privacy. QUALIFICATIONS: BS/BA degree (preferred) High School Diploma (or equivalent) required. 2+ years of medical industry related experience - pathology preferred. Previous data entry experience is required. KNOWLEDGE, SKILLS, AND ABILITIES Trained on all product types and able to QC with high accuracy and efficiency consistently. Ability to handle most escalations, discrepancies, and holds. Firm understanding and knowledgeable in all aspects of the Sample Review process and SOPs. Typing speed of at least 45wpm with high accuracy. Excellent oral and written communication. Excellent critical
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TITLE: Senior Workday Platform Engineer
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $129K-$161K
POSTED: 2026-05-12
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5993464004
EXCERPT: Senior Workday Platform Engineer US Remote We are seeking a hands-on Senior Workday Platform Engineer within the G&A IT Applications team to serve as the primary technical owner of the Workday platform across HCM, Payroll, Recruiting, Prism Analytics, Illuminate (AI/ML), integrations, security, and release management. This is a builder-first role. You will configure, develop, integrate, and operate within Workday while partnering closely with HR, Payroll, Finance, and IT stakeholders. You own the technical platform layer configuration, integrations, security architecture, governance, and release discipline, while HR and Payroll retain ownership of sensitive data and business policy logic. Key Responsibilities Platform Ownership & Delivery: - Own technical execution across Workday HCM, Payroll, Recruiting, Prism Analytics, and Illuminate. - Translate business requirements into phased technical delivery plans. - Manage sandbox strategy, tenant lifecycle, and biannual release readiness. Hands-On Configuration & Development: - Configure HCM and Recruiting modules.Build advanced reports (matrix, composite, BIRT), calculated fields, validations, and business process frameworks. - Leverage Workday Extend to design and build lightweight custom applications that enhance core workflows. - Maintain scalable security models and governance standards. Integrations & Architecture: - Build and maintain integrations (EIB, Studio, REST/SOAP APIs, RaaS). - Integrate with applications like ERP, identity providers, benefits carriers, and third-party systems. - Ensure secure, reusable integration frameworks with monitoring and error-handling discipline. Analytics, AI & Automation: - Implement and manage Workday Prism Analytics datasets and dashboards. - Enable Workday Illuminate capabilities and intelligent workflows. - Drive automation while maintaining audit and compliance standards. Security & Compliance:
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TITLE: Senior Quality Clinical Data Abstractor
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-09
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6017432004
EXCERPT: Senior Quality Clinical Data Abstractor US Remote POSITION SUMMARY: Perform high-quality medical record abstraction by combining proficient-level experiences in data management and software with medical terminology, medical coding, information encoding, and analytical capabilities. Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: - Data Abstraction: Accurately review, interpret, and abstract clinical patient data from various electronic health record (EHR) systems, paper charts, and other source documents in accordance with defined project or research protocols, clinical, data, and technical specifications, and dictionaries. - Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data points from unstructured text to standardized machine readable data in one common database schema. - Electronic Data Capture (EDC): Utilize specialized data management software (e.g., REDCap, registries, and custom built EDC systems) to enter, track, and maintain the integrity of clinical data encoded into queryable databases. - Technical Support: Aid cross-functional teams in translating clinical and data abstraction and encoding requirements. Support prompt engineering and design for all AI and LLM initiatives. - Data Management: Apply and support establishing program specific clinical data management best practices (CGDMP) and good clinical practice (GCP) during the abstraction and encoding process resulting in accurate, legible, contemporaneous, original, attributable, complete and consistent for end-to-end ETL workflows. - Quality Assurance and Control: Apply industry standard best practices for utilizing real-world data for research, quality monitoring, and regulatory reporting using
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TITLE: Program Manager
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-05-15
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5989220004
EXCERPT: Program Manager US Remote POSITION SUMMARY: The Program Manager will lead cross-functional programs supporting product development initiatives at the Boulder, CO site. Projects and programs may include development, validation, and regulatory submission of diagnostic products; support of biopharma companion diagnostic (CDx) partnerships; and product sustainment and lifecycle management efforts. This role is responsible for driving execution across product development cross functional teams, including R&D, software, manufacturing, laboratory operations, quality, regulatory, clinical development, commercial, alliance management, and external partners, to ensure timely, compliant delivery of key milestones and contractual commitments. The Program Manager will partner with functional leaders and stakeholders to translate product strategy into executable plans, manage cross-functional dependencies, and maintain alignment across internal and external stakeholders. This role requires strong program management fundamentals, experience and comfort operating in regulated environments, and the ability to coordinate complex, multi-disciplinary efforts simultaneously. The Program Manager will drive, communicate, and engage all project partners to enable accountability, problem solving, and on-time/within-budget delivery for simultaneous projects and programs. Success in this role requires onsite engagement (up to 25% travel) to facilitate rapid decision-making, build alignment, and resolve issues in a highly collaborative, fast-paced setting. This position reports to the Associate Director of Program Management. PRIMARY RESPONSIBILITIES: - Drive end-to-end execution of product development programs, including planning, scheduling, resource coordination, and risk management across assay, software, and systems development, ensuring alignment with regulatory and business requirements. - Support regulatory product development activities, ensuring alignment with regulated processes and quality systems, including design control processes (ISO
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TITLE: Staff Salesforce Architect, Sales & Service Cloud
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (unspecified)
SALARY: $153K-$191K
POSTED: 2026-02-06
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5795479004
EXCERPT: Staff Salesforce Architect, Sales & Service Cloud Austin, TX The Opportunity We are seeking an exceptional Staff Salesforce Architect to lead the design and evolution of our Sales Cloud and Service Cloud platforms. In this strategic role, you'll own the technical architecture, govern platform standards, and drive transformation initiatives that impact thousands of users across go-to-market and customer success functions. You'll be our technical authority on Salesforce best practices, scalability, and innovation. What You'll Do Platform Architecture & Governance (35%) - Design end-to-end solutions integrating Sales and Service Cloud; establish metadata frameworks, custom objects, and data models for scalability - Define platform standards, coding guidelines, and integration patterns; ensure compliance with Salesforce Governor Limits and platform constraints - Lead org hygiene initiatives, technical debt reduction, and long-term roadmap evolution Solution Design & Implementation (40%) - Architect complex workflows, automation, omni-channel, and AI-driven capabilities (Einstein Analytics, Einstein Copilot) - Design secure integrations (MuleSoft, AWS, REST/OAuth) between Salesforce and enterprise systems - Lead implementation of key initiatives (data cloud, person accounts, skill-based routing) from design through production Mentorship & Technical Leadership (25% - Guide Salesforce developers and admins; conduct design reviews and architecture validation - Partner with product, business systems, and engineering leadership on roadmap alignment What You'll Bring Required: - 10+ years of Salesforce architecture and implementation experience, with deep expertise in Sales and Service Cloud - Expert-level knowledge of Apex, Lightning Web Components (LWC), Flows, and SOQL optimization - Proven ability to design secure, scalable integrations (REST APIs, OAuth, SSO,
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TITLE: Senior CTMS Delivery Product Manager (Salesforce)
EMPLOYER: Natera, Inc.
LOCATION: Austin, TX (unspecified)
SALARY: $141K-$176K
POSTED: 2026-02-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5803019004
EXCERPT: Senior CTMS Delivery Product Manager (Salesforce) Austin, TX Role Overview The Senior CTMS Delivery Product Manager is responsible for technical delivery, system design coherence, and architectural integrity of the Salesforce-based Clinical Trial Management System (CTMS), including Cloudbyz components. This role sits within the technology organization and serves as the technical design authority for CTMS delivery , ensuring that ClinOps-owned business decisions and outcomes are implemented using a holistic, end-to-end system architecture that supports scalability, compliance, and long-term maintainability. The role focuses on how CTMS changes are designed and delivered technically, while system roadmap and final business decisions remain with Clinical Operations , consistent with the CTMS governance model . Key Responsibilities CTMS Technical Architecture & System Design (IT Delivery Accountability | ClinOps Consulted) - Act as the CTMS Technical System Architect for Salesforce and Cloudbyz implementations - Maintain a holistic architectural view of the CTMS platform across: - Study, site, subject, and financial modules - Integrations with EDC, eTMF, IRT, ERP, and analytics systems - Evaluate proposed changes for cross-module, cross-study, and cross-system impacts - Define and enforce technical design standards , data models, and integration patterns - Prevent fragmented, study-specific configurations that introduce technical debt Architectural accountability is technical delivery-focused and does not include ownership of business processes, system outcomes, or regulatory risk, which reside with ClinOps . CTMS Delivery & Execution (IT Accountable | Cloudbyz Responsible under IT) - Serve as the IT delivery owner for CTMS enhancements and platform changes - Execute delivery against a ClinOps-defined and
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TITLE: Senior Clinical Scientist, Oncology
EMPLOYER: Natera, Inc.
LOCATION: United States (unspecified)
SALARY: $142K-$178K
POSTED: 2026-03-13
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5824682004
EXCERPT: Senior Clinical Scientist, Oncology United States POSITION SUMMARY: We are seeking a Senior Clinical Scientist, Oncology to drive clinical development strategy and trial execution for our molecular residual disease (MRD) monitoring portfolio. This ownership role applies oncology domain expertise to integrate our tumor-informed cfDNA platform into standard-of-care clinical protocols. As a clinical trial lead, you will design and execute MRD study protocols that outpace the competitive landscape by substituting clinical assumptions with empirical validation data. You will operate cross-functionally across medical, commercial, and biostatistics lines to eliminate operational latency and advance trial performance. PRIMARY RESPONSIBILITIES: Study Concept and Protocol Development - Author robust trial concepts, specifying clinical design parameters, schedules of assessments, objectives, endpoints, and patient eligibility criteria - Synthesize protocol requirements from investigators, clinical partners, and regulatory bodies, resolving conflicting operational priorities by anchoring team alignment strictly in data - Write complex study protocols and deliver technical documentation to resolve health authority queries precisely and rapidly - Deliver technical protocol validation and design training modules for internal teams and contract research organizations (CROs) Operational Trial Alignment - Partner with Clinical Operations to configure study-specific case report forms (CRFs) and drive protocol conformity during user acceptance testing - Author technical sections of CRF completion guidelines and verify that study manuals align directly with trial protocol specifications - Lead technical data exchanges during investigator meetings, pre-site selection reviews, and site initiation visits to maximize protocol compliance - Serve as the authoritative Clinical Science representative across internal study team gates and external
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TITLE: Sr Clinical Data Abstractor
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: Not disclosed
POSTED: 2026-06-09
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6017426004
EXCERPT: Sr Clinical Data Abstractor US Remote POSITION SUMMARY: Perform high-quality medical record abstraction by combining proficient-level experiences in data management and software with medical terminology, medical coding, information encoding, and analytical capabilities. Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: - Data Abstraction: Accurately review, interpret, and abstract clinical patient data from various electronic health record (EHR) systems, paper charts, and other source documents in accordance with defined project or research protocols, clinical, data, and technical specifications, and dictionaries. - Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data points from unstructured text to standardized machine readable data in one common database schema. - Electronic Data Capture (EDC): Utilize specialized data management software (e.g., REDCap, registries, and custom built EDC systems) to enter, track, and maintain the integrity of clinical data encoded into queryable databases. - Technical Support: Aid cross-functional teams in translating clinical and data abstraction and encoding requirements. Support prompt engineering and design for all AI and LLM initiatives. - Data Management: Apply and support establishing program specific clinical data management best practices (CGDMP) and good clinical practice (GCP) during the abstraction and encoding process resulting in accurate, legible, contemporaneous, original, attributable, complete and consistent for end-to-end ETL workflows. - Quality Assurance and Control: Apply industry standard best practices for utilizing real-world data for research, quality monitoring, and regulatory reporting using technical
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TITLE: Director, Clinical Science
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $193K-$241K
POSTED: 2026-05-05
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5987844004
EXCERPT: Director, Clinical Science US Remote POSITION SUMMARY: We are seeking a Director, Clinical Science to architect trial strategies and protocol execution for our oncology molecular diagnostics portfolio, with a dedicated focus on signal Studies and pipeline expansion. This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA) technology, transforming population scale genomic profiles into standard-of-care screening benchmarks. Reporting directly to the Senior Director of Clinical Science, you will lead the strategic alignment and tactical delivery of early and late-stage oncology diagnostics protocols. Operating with an active builder mindset, this position co-develops clinical program strategy and drives collaborative execution across clinical development, clinical operations, biostatistics, and translational data science teams. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture - Design robust clinical study concepts, specifying overall design parameters, schedules of assessments, trial objectives, clinical endpoints, and patient eligibility criteria - Lead clinical development activities and protocol design for oncology Signal Studies and portfolio development - Collaborate cross-functionally to author clinical study protocols, informed consent documents, and technical amendments for internal governance review - Deliver technical protocol validation training to internal teams and contract research organizations (CROs), and guide case report form (CRF) layout configurations - Ensure study manuals conform directly to protocol specifications and engage primary clinical investigators during initial trial design phases Data Interrogation and Cross-Functional Alignment - Synthesize protocol requirements from investigators, clinical partners, and regulatory bodies, resolving conflicting operational priorities by anchoring team alignment strictly in data - Partner with cross-functional technical teams to execute
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TITLE: Principal Clinical Scientist, ECD
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $188K-$235K
POSTED: 2026-05-01
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5984096004
EXCERPT: Principal Clinical Scientist, ECD US Remote POSITION SUMMARY: We are seeking a Principal Clinical Scientist to lead execution of key components of clinical development for our early cancer detection (ECD) program. This role is central to leading study execution, clinical data review, study design, and generation of scientific insights across multiple studies. The successful candidate will contribute meaningfully to clinical development strategy through hands-on study leadership, cross-functional execution, and data-driven decision-making. You will serve as a clinical science lead within cross-functional teams-partnering closely with Clinical Operations, Biostatistics, Medical Affairs, and Regulatory to drive study execution, identify risks and opportunities, and contribute to clinical development strategy through study-level leadership and scientific insight. This role is best suited for a clinical scientist who enjoys remaining closely involved in study execution, clinical data review, and cross-functional problem solving while contributing to broader clinical development discussions and strategy. Location: San Carlos, CA or Remote, USA (West Coast or Mountain time zones preferred) PRIMARY RESPONSIBILITIES: Lead Clinical Development & Study Design - Lead substantial aspects of ECD clinical studies or multiple studies - Drive study design, including objectives, endpoints, eligibility criteria, and schedules of assessments - Author and review protocols, ICFs, CRFs, and study documents - Contribute meaningfully to clinical development strategy and study-level decision-making - Contribute to process improvements and development of best practices Drive Data Review & Strategic Insight - Lead medical and clinical data review to ensure data quality and integrity - Analyze complex datasets to identify trends, risks, and opportunities -
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TITLE: Organ Health Specialist – Abdominal Transplant (Southeast Central)
EMPLOYER: Natera, Inc.
LOCATION: Atlanta, GA; Birmingham, AL; Jackson, MS; Memphis, TN (unspecified)
SALARY: $180K-$200K
POSTED: 2026-06-03
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/6010923004
EXCERPT: Organ Health Specialist – Abdominal Transplant (Southeast Central) Atlanta, GA; Birmingham, AL; Jackson, MS; Memphis, TN Territory : Georgia, Mississippi, Alabama, Arkansas, Memphis (TN), and Shreveport (LA). Ideally, candidates should be centrally located near a major airport hub within the region (e.g., Atlanta, Birmingham, Memphis, or Little Rock). About the Role We are seeking an experienced, high-performing Organ Health Specialist (OHS) - Abdominal Transplant to join our rapidly growing Organ Health Sales team. In this role, you won't just be managing a territory-you will be championing a shift in how transplant patients are cared for across the Deep South and Delta regions. By cultivating deep clinical relationships with transplant centers, nephrologists, and surgeons, you will drive the adoption of our cutting-edge diagnostic and genetic testing portfolios. We are looking for critical thinkers who can synthesize complex clinical data and navigate institutional barriers. If you possess the strategic agility to pivot approaches in a highly competitive market and want to make a definitive impact on long-term graft survival, we want you on our team. Our Portfolio - Prospera: Our advanced, non-invasive donor-derived cell-free DNA (dd-cfDNA) blood test designed to detect early signs of transplant rejection. - Renasight: A comprehensive genetic testing panel that identifies hereditary causes of kidney disease, allowing for early, precise intervention. Primary Responsibilities - Drive Market Adoption: Exceed regional sales goals by integrating Prospera and Renasight into the standard protocol of leading transplant centers and academic medical institutions across the territory. - Demonstrate Strategic Agility: Develop and execute
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TITLE: Associate Director, Real-World Evidence & Epidemiology
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $176K-$220K
POSTED: 2026-04-30
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5984094004
EXCERPT: Associate Director, Real-World Evidence & Epidemiology US Remote POSITION SUMMARY: We are seeking a Principal Clinical Scientist / Associate Director of Real-World Evidence & Epidemiology to drive observational evidence strategy for our Early Cancer Detection (ECD) portfolio. Population-scale liquid biopsy screening requires robust real-world evidence demonstrating clinical utility, clinical decision-making impact, and downstream patient outcomes. This ownership role uses real-world datasets to accelerate standard-of-care implementation across oncology diagnostics. Working with a builder mindset, you will partner across Clinical Science, Medical Affairs, Market Access, and Data Science to convert population-scale observational data into actionable clinical implementation strategies. PRIMARY RESPONSIBILITIES: Epidemiology and Observational Research Strategy - Lead the design, protocol development, and execution of prospective observational studies, registries, and retrospective database assessments across early cancer detection programs - Shape post-market evidence generation strategies by isolating critical clinical utility and implementation hurdles that can be resolved via real-world data assets - Translate clinical and market requirements into rigorous, practical study designs, specifying target populations, clinical endpoints, and analytic frameworks - Systematically identify and mitigate sources of bias, confounding factors, and missing data variance inherent in real-world healthcare datasets - Design protocols evaluating clinical utility across diverse populations, ensuring the data generated directly supports precision interventions for individual patients and families Cross-Functional Scientific Leadership - Partner across Clinical Science, Medical Affairs, Product Management, and Market Access to prioritize evidence generation initiatives based on regulatory and clinical urgency - Collaborate with Biostatistics and Data Science to engineer statistical analysis plans, interpret data findings, and deliver
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TITLE: Staff AI-Native Platform Engineer
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $152K-$190K
POSTED: 2026-03-31
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5838483004
EXCERPT: Staff AI-Native Platform Engineer US Remote Staff AI-Native Platform Engineer (L5) Location: US - Remote Experience: 8+ years in Cloud/Platform Engineering or Infrastructure, with a proven track record of leading cross-functional initiatives and influencing organizational AI strategy. About the Role We are looking for a visionary Staff AI-Native Platform Engineer to lead the evolution of our technical foundation. In this high-impact role, you will move beyond traditional automation to architect an AI-native ecosystem that integrates Generative AI into every layer of our Development Platform. As a technical leader within the Platform organization, you won't just be maintaining infrastructure, you will be reimagining the developer experience (DevEx) . You will be the primary advocate for GenAI, fostering a culture of “AI-first” engineering by building agentic workflows that accelerate Cloud Orchestration, CI/CD, Observability, and FinOps. We need a creative engineer who can bridge the gap between cutting-edge LLM capabilities and robust, production-grade platform tooling. What You'll Do Architect AI-Integrated Infrastructure - AI-First Development Platform: Design and build unified interfaces where AI agents manage complex tasks like environment provisioning, automated PR reviews, and self-documenting codebases. - Intelligent Orchestration: Embed AI-driven intelligence into CI/CD pipelines and Observability stacks to enable predictive scaling, automated incident triage, and self-healing systems. - Autonomous FinOps: Evolve AI-assisted FinOps workflows to automate cost attribution, anomaly detection, and optimization recommendations across AWS and other cloud environments. - Governance & Guardrails: Implement AI-driven governance to ensure architectural standards and security policies are met without slowing down developer velocity. Elevate Developer Experience
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TITLE: Associate Director, Clinical Science
EMPLOYER: Natera, Inc.
LOCATION: US Remote (remote)
SALARY: $175K-$218K
POSTED: 2026-05-05
APPLY_URL: https://job-boards.greenhouse.io/natera/jobs/5987840004
EXCERPT: Associate Director, Clinical Science US Remote POSITION SUMMARY: We are seeking an Associate Director, Clinical Science to architect trial strategies and protocol execution for our oncology biobanking studies and specimen repositories. This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA) technology, transforming population-scale genomic profiles into standard-of-care screening benchmarks. Reporting directly to Neda Huseinovic, Senior Director of Clinical Science, you will lead the strategic alignment and tactical delivery of complex biobanking clinical protocols. Operating with an active builder mindset, this position co-develops clinical program strategy and drives collaborative execution across clinical operations, biostatistics, and translational data science teams, directly managing the clinical scientists embedded within the biobanking workstream. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture - Design robust clinical study concepts, specifying overall design parameters, sample-size logic, schedules of assessments, trial objectives, clinical endpoints, and patient eligibility criteria - Lead clinical development activities and protocol design for oncology biobanking studies and biospecimen repository portfolios - Collaborate cross-functionally to author clinical study protocols, informed consent documents (ICFs), and technical amendments for internal governance review - Deliver technical protocol validation training to internal teams and contract research organizations (CROs), and guide case report form (CRF) layout configurations - Ensure study manuals conform directly to protocol specifications and engage primary clinical investigators during initial trial design phases Data Interrogation and Cross-Functional Alignment - Synthesize protocol requirements from investigators, clinical partners, and regulatory bodies, resolving conflicting operational priorities by anchoring team alignment strictly in data - Partner across cross-functional
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