Freenome jobs - 24 jobs

About this opportunity: At Freenome, we are seeking a Lab IT Helpdesk to help grow the Freenome IT team. The ideal candidate is a tech-savvy problem solver who thrives on helping others. This person is responsible for providing primary support for our lab IT infrastructure and resolving systems issues. You are passionate about technology and healthcare, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Director of IT. This role will be an Onsite role based in our Brisbane, California headquarters. What you'll do: Provide primary support for lab IT infrastructure and systems issues/requests, ensuring incidents are prioritized and resolved within SLA guidelines. Perform onsite troubleshooting of computer systems, networks, hardware, and software in a laboratory environment. Install, configure, and manage lab-related software, licenses, and workstations (physical and virtual). Collaborate with Network and System Administrators to maintain and develop solutions in a regulated environment. Record events, problems, and resolutions in our ticketing system (Freshservice). Create and manage user accounts, permissions, and access controls. Maintain comprehensive documentation for configurations, troubleshooting steps, and routine procedures. Assist with hardware and software upgrades in collaboration with cross-functional departments to ensure minimal disruption to lab operations. Support shared lab workstations and environments where uptime is critical and sessions may need to remain active. Assist with endpoint provisioning, imaging, and redeployment for lab and office devices. Follow change control and validation-aware practices when working on systems in production lab spaces. Participate in on-call or extended coverage rotations as required to support lab operations. Must haves: 3+ years of experience as a Help Desk Specialist or related IT Customer Support role. Experience with Windows platforms, specifically Windows 10/11 support. Experience with Entra id and ticketing systems. Experience with Mobile Device Management (MDM) tools (e.g., Manage Engine, Jamf). Ability to work onsite Mon-Sat (specific shift hours can be defined, e.g., 7AM-3PM or 10AM-6PM). 5 days a week. Excellent communication and customer service skills with the ability to explain technical solutions to non-technical staff. Physical ability to lift/move hardware and navigate a lab layout (e.g., under-bench cabling). Ability to prioritize requests based on operational impact, especially in lab/production settings. Strong troubleshooting skills across hardware, OS, peripherals, and user access issues. Comfortable working in environments with noise, PPE requirements, and restricted access areas. Nice to haves: Windows experience in a Lab environment. Experience in diagnostic labs or a regulated environment (e.g., CLIA, FDA, HIPAA). Industry certifications such as ITIL, CompTIA A+, or Microsoft Certified Professional. Basic networking knowledge and experience with Active Directory. Scripting experience (PowerShell, Python, Bash) to automate tasks. Additional information: Contractors may be hired through a third-party provider and will be considered contingent workers. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: At Freenome, we are seeking a Senior Computational Biologist, Assay Development to help grow the Freenome's Computational Biology, Assay Development (CBAD) team. As part of our team, you will apply your scientific expertise to the development of early, noninvasive tests for cancer detection. With a strong background in bioinformatics, statistics, and molecular biology, you will develop, write, and execute analysis plans and reports for the development and characterization of Freenome's in vitro diagnostic devices and regulatory filings. You will work closely and cross-functionally with many teams, including Regulatory and Quality, Molecular Research and Development, Laboratory Operations, Biostatistics, Computational Science, and Engineering to enable the successful development of multiple molecular assays as part of Freenome's diagnostic products. The role reports to the Director of Computational Biology. This role can be Hybrid (2-3 days onsite in Brisbane, CA) or Remote role. What you'll do: * Plan and execute development experiments for Freenome's multiomics cancer screening tests. * Partner cross-functionally with computational, development, regulatory, and quality leaders to develop and execute a regulated development strategy working toward FDA approval. * Use your quantitative skills to develop computational methods and interpret complex experimental results in order to optimize and validate innovative technology for sample collection, preparation, and detection. * Develop and execute appropriate experimental design and analysis plans for Development, Verification, and Validation studies, closely partnering with Biostatistics, Development, and Pre-Analytics teams. * Work closely with molecular and computational research teams developing Freenome's IVD products for blood-based molecular assays involving cell-free DNA. * Impact patient lives through the development and launch of high quality cancer screening technologies. Must haves: * Post-graduate degree (MS or PhD) in statistics, computational biology, bioinformatics, cancer biology, or related quantitative field. * 3+ years of industry experience. * Experience with molecular biology and next generation sequencing. * Experience in experimental design and analysis of high-throughput, quantitative technologies. * Familiarity with and ability to select and leverage bioinformatics tools for the above molecular assays. * Experience in applied statistics, such as in hypothesis testing, GLM, and appropriate use of simulation. * Expertise in data analysis and visualization using R (tidyverse), or Python statistical packages (Numpy, Matplotlib, Pandas), or equivalent, under version control. * Excellent oral and written communication skills to communicate to scientific and broader audiences, with keen attention to detail. * Ability to work on a cross-functional team in our highly collaborative environment, working with both computational and experimental scientists. Nice to haves: * Experience in the development of diagnostic devices in a regulated environment (PMA, 510(k), CE-IVD) preferred. * Experience with a variety of NGS methods (e.g., WGS, target capture with UMI, bisulfite sequencing, RNA-seq). Benefits and additional information: The US target range of our base salary for new hires is $161,925 - $247,000. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. * Family & Medical Leave Act (FMLA) * Equal Employment Opportunity (EEO) * Employee Polygraph Protection Act (EPPA) #LI-HYBRID

About this opportunity: As a Supervisor, R&D Labs at Freenome, you will oversee our Research & Development laboratory operations. The ideal candidate is a proactive leader with a passion for scientific innovation and operational excellence. You will ensure the lab operates seamlessly and scales effectively amidst growth and increasing complexity. Your duties will encompass refining processes, upholding a high-performance work culture, and driving collaboration with Facilities, Supply Chain, and the Clinical Laboratory to meet the evolving needs of our R&D operations. You are passionate about driving scientific advancements and operation efficiencies, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Senior Manager, Development & Scientific Operations. This role will be an onsite role based in our Brisbane, California headquarters. What you'll do: Manage and build a high-performing team, providing day-to-day guidance and support to foster a culture of continuous improvement and professional development. Implement and maintain processes for cold storage organization, lab safety, equipment scheduling, lab notebook auditing, and general lab upkeep. Act as a key liaison with Supply Chain, Software, & R&D Science teams to integrate requirements and processes, ensuring auditability and documentation best practices. Partner with Supply Chain to ensure adequate supplies of consumables and reagents. Onboard new employees into the lab. Assist with Forecasting and tracking of lab budget. Collaborate with R&D teams in the planning and execution of the physical expansion of the R&D Lab in collaboration with Facilities. Lead initiatives to enhance laboratory capabilities and efficiency. Help drive safety culture and maintaining it as a top priority. Ability to identify critical equipment issues and drive CAPA's to completion for the betterment of the department. Collaborate with Facilities, SciOps and Automation Service teams to maintain and monitor R&D cold storage, ensuring equipment-failure contingency plans are in place. Continuously assess team member proficiency to identify training needs and ensure team members receive regular in-service training. Contribute to and implement the laboratory's strategic vision and goals in alignment with organizational objectives. Actively participate in laboratory operations, providing hands-on support to ensure continuity and efficiency in lab activities. Must haves: Bachelor's in clinical laboratory science, biological science or a related discipline and 6+ years training/experience. Exceptional communication and collaboration skills. Proven track record of championing processes that improve efficiency in the lab. Benefits and additional information: The US target range of our base salary for new hires is $91,800 - $129,675. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: Freenome is seeking a Clinical Laboratory Associate (CLA) to assist our Clinical Laboratory Scientists (CLSs) and support the daily operations of the Clinical Laboratory under direct supervision of the Clinical Laboratory Scientist. It is important to our mission to provide quality samples to process downstream for quality analysis and results. The role reports to a Supervisor in the Clinical Lab. This role will be an Onsite role based in our Brisbane, California headquarters. The standard hours of this position are 7:30am-4:00pm. The working hours are subject to change to support special projects. Flexibility to support these projects is required for this role. Sufficient notice will be provided. Standing or sitting for extended periods may be necessary. What you'll do: Performing equipment maintenance according to the laboratory's standard operating procedures (SOPs) for machines and devices including, but not limited to, the following: centrifuges, freezers, refrigerators, pipettors, microplate readers, NovaSeq units, immunoassay instruments and equipment, Agilent Bravo units, Hamilton units, and work cells, as needed Creating sample batches, printing labels, and labeling tubes and plates Maintaining sufficient inventory of material, supplies, and equipment in the laboratory for performance of duties Documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications Assisting the CLS with preparation and aliquoting of reagents Assisting the CLSs during sample testing Assisting the CLSs with quality control (QC) and quality assurance (QA) functions Participating in projects under the supervision of a CLS or supervisor along with maintaining quality and an efficient workflow in daily duties Ensuring on-time calibration of laboratory equipment is scheduled and performed Setting up the Hamilton and assisting with Hamilton automated procedures Setting up the work cell and assisting with work cell automated procedures Must haves: Bachelor of arts or bachelor of science degree in biomedical laboratory science, clinical science, or a related field The ability to prioritize tasks with a high emphasis on quality Strong organizational skills and meticulous attention to detail High attention to detail The ability to work as part of a team within a highly collaborative environment Nice to haves: 1 year of work experience in a clinical laboratory setting Additional information: Contractors may be hired through a third-party provider and will be considered contingent workers. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: Freenome is looking for a Vice President, Digital Health, as a key member of our rapidly developing Commercial and Product teams. The ideal candidate will be a visionary leader with hands-on experience in defining, developing, and deploying a cohesive digital platform that enables and scales cutting-edge diagnostic solutions within complex healthcare ecosystems, enhancing interactions with patients and providers. This role offers a unique opportunity to build and deploy the digital infrastructure necessary for this game-changing early disease detection technology to be seamlessly integrated into clinical practice. In this role, you will be instrumental in bridging the gap between Freenome's cutting-edge science and its practical application in physician offices and health systems, ultimately maximizing patient adherence and test utilization. You will contribute to guiding and refining company-level strategy. Your commitment to innovation and seamless user experience will significantly contribute to our growth and our mission to outpace cancer with early detection. This role will report to the Chief Commercial Officer and will serve as a vital part of the Commercial Leadership Team. This is a remote role with the requirement to travel up to 30% of the time. What you'll do: Digital Health Platform Strategy & Development Platform Strategy Development and Deployment: Define and drive the long-term vision and architecture for Freenome's digital health platform. This includes performing Voice of the Customer (VOC), maintaining industry and competitor awareness, incorporating innovative/pioneering thinking (true innovation), integrating advisory committee feedback, and interfacing with core technology capabilities to support the long-term vision of rules-based medicine programs. Feature Design and Development: Lead the design and development of critical platform features and functions, such as patient identification, education modules, provider engagement tools, EHR integration, and adherence management systems. Function Performance and Roadmap: Oversee the ongoing function performance management and maintenance of the improvement roadmap for all digital platform features. Program Performance & Engagement Overall Program Performance Achievement: Accountable for the achievement of digital health program performance goals, ensuring the platform effectively drives utilization, adherence, and customer satisfaction. Program Performance Metric and Goal Development: Define, track, and manage key performance indicators (KPIs) and goals for all digital health programs. KOL and Advisory Committee Engagement: Lead KOL and Advisory Committee engagement for program development, design validation, and establishing program credibility with clinical and technical stakeholders. Medical Affairs Partnership: Proactively partner with Medical Affairs to align the digital platform with the publication strategy, ensuring features support evidence design and development needs. Continuous Improvement: Evaluate program effectiveness and work with the technical team to continuously improve program function and scope. Clinical Integrity Interoperability and Integration: Act as a primary interface with health-system IT leaders, clinical operations, and informatics teams to scope and negotiate integration requirements. Clinical Strategy Representation: Represent Freenome's clinical strategy in discussions around interoperability, FHIR/HL7 capabilities, ordering modules, clinical decision-support, and results workflows. Clinical Workflow Translation: Translate Freenome's diagnostic science into practical platform features such as risk-based prompts, decision-support logic, and results interpretation pathways. Customer Education: Create crisp education/messaging on the clinical and economic impact of Freenome tests, and help inform customer decision-making to improve population health initiatives. Clinical Understanding: Demonstrate a keen understanding of how PCPs and specialists evaluate risk, order tests, and interpret results. Compliance and Validation: Ensure all data flows, clinical algorithms, and decision-support tools comply with best practices and clinical guidelines. Must haves: Bachelor's degree in a technical or relevant field. 15+ years of progressive commercial or product leadership experience in diagnostics, pharmaceuticals, or biotech, with significant focus on digital health, health IT, or clinical informatics. 10+ years in senior leadership roles, with direct responsibility for designing, launching, and scaling digital health platforms for clinical use. Demonstrated ability to build executive-level relationships with C-suite leaders and key decision-makers across health systems and provider networks. Deep expertise in healthcare data standards (FHIR, HL7), EHR integration, and clinical decision support systems. Proven track record of identifying and negotiating strategic partnership opportunities that expand distribution, access, and ecosystem impact. Strong entrepreneurial mindset and passion for pioneering new digital solutions in a complex, regulated environment. Demonstrated ability to closely collaborate cross-functionally to build and launch digital platforms in a matrixed organization. Ability to craft and clearly convey the company's story compellingly to diverse audiences. Nice to haves: Advanced degree (MBA, MS in Health Informatics, or similar). Experience with AI/ML-driven decision support tools and rules-based clinical programs. Experience in oncology or preventative screening. SF Bay Area residency is a plus but not mandatory. Benefits and additional information: The US target range of our base salary for new hires is $262,650 - $383,775. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-REMOTE

About this opportunity: At Freenome, we are seeking a Staff Development Scientist to join Freenome's Genomics Development team. The ideal candidate will serve as a technical expert in end to end product development for our Genomic workflows.. You will collaborate with Molecular Research, Computational Science, Validation and Verification, Automation, Manufacturing, Quality, Regulatory & Product Management teams to develop and transfer technologies into a regulated, high-throughput environment and contribute to Freenome's multiomic product portfolio aimed at early cancer detection. The role reports to the Senior Director, Development. This role will be an on-site role based in our Brisbane, California headquarters. What you'll do: Provide expertise in prototype evaluation, design, development and subsequent transfer of NGS based methodologies and assays. In close partnership with cross functional teams, influence product design,IP, and business strategy by providing sound technical input that balances technical and business objectives. Ensures Design Control framework is adopted and implemented through the Product Development life cycle. Serve as the cross-functional liaison representing Development. Lead multiple projects/programs simultaneously. Take lead on implementing ideas or process improvements with a significant impact on Freenome's technology platform and the business as a whole, and take full accountability for their overall technical direction. Serves as a thought partner for internal and external stakeholders and be called upon as a technical subject matter expert. Set technical direction for programs and adapt communication style to effectively communicate the depth of the work to compel and influence diverse audiences. Meticulously establish and document procedures and processes that have visible impact on the strategic goals of the company. Must haves: Bachelor's or Master's degree in molecular biology, biochemistry, genetics, or a related field with 12+ years of experience or PhD with 8+ years of experience in Product Development in the molecular diagnostics industry. Deep expertise in running and developing automated molecular biology and biochemistry assays for LDT and/or IVD products.Proven track record of end to end product development working on multiple programs simultaneously. Excellent communications skills and stakeholder management skills. Nice to haves: Experience with IVD products. Experience working in a regulated laboratory environment (CLIA, GLP/GCLP, IVD development). Experience with NGS assays along with strong expertise with analysis and interpretation of NGS data. Benefits and additional information: The US target range of our base salary for new hires is $166,175 - $237,825. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: Our Site Reliability Engineering (SRE) team is a new and critical function at Freenome. As a founding member of the team, you'll help define the culture and build the systems that keep our regulated, cloud-based production environments reliable as we transition from research to commercial operations. This is an opportunity to do meaningful engineering work that will directly save lives. We value: Reliability as a product feature. Continual improvement and learning. Automate all the things! Technical simplicity and clarity. Blameless postmortems and transparent communication. As a Site Reliability Engineer, you will help design, implement, and operate observability, reliability, and incident management systems and practices across our clinical lab systems and regulated commercial workloads. You'll partner with engineering teams to define service-level indicators (SLIs), objectives (SLOs), and error budgets; build runbooks and operational playbooks; and develop the monitoring and automation needed to ensure that our systems are reliable and compliant. This will also include contributions to system code, Infrastructure deployments and automation. This role is ideal for an engineer with experience running production workloads in the cloud, who is excited to build an SRE practice from the ground up in a regulated environment. The role reports to the Director, Cloud Infrastructure. What you'll do: Define and implement observability practices (metrics, traces, dashboards, logs, alerts) for production systems. Partner with product, engineering, and lab teams to develop and maintain incident response playbooks and escalation procedures. Partner with engineering teams to define SLIs/SLOs and establish error budgets. Participate in on-call rotation for production systems, champion a focus on automation and self-healing. Contribute to production deployment and change-management processes that meet FDA and compliance requirements. Automate operational tasks, reducing manual intervention. Contribute to production systems and designs with the goal of improving reliability. Use Infrastructure as Code (IaC) to manage and deploy team owned infrastructure and subsystems. Help build out the SRE practice. Communication and Collaboration: Work closely with engineering, product, and lab teams to understand service reliability needs. Partner with TPMs, RA/QA, and compliance stakeholders to align operational practices with regulatory requirements. Participate in cross-functional incident reviews and postmortems. Share knowledge and document operational standards for consistency and onboarding. Design and run fire drills / tabletop exercises as well as disaster recovery exercises. Culture: Model Freenome's values and principles in your work and interactions. Promote a collaborative, reliable engineering culture across product, infra, and lab engineering teams. Contribute to documentation, runbooks, and operational standards. Foster a culture of accountability, learning, and psychological safety. Technical Leadership: Independently drive reliability improvements in scoped systems or services. Provide mentorship to peers on observability, incident management, and operational best practices. Help build and evolve Freenome's reliability practices and contribute to team strategy discussions. Must haves: Bachelor's degree in Computer Science, Engineering, or equivalent experience. 5+ years in software engineering or Infra/DevOps/SRE roles (Python or Go are what we currently use). Experience deploying cloud infrastructure via automation (e.g. Terraform, Pulumi, Bicep/ARM, etc.). Incident management experience in cloud/software engineering as well as familiarity with incident management platforms (e.g., Incident.io, ServiceNow, Opsgenie, Pagerduty, etc.). Hands-on experience operating production workloads in cloud environments. Familiarity with Kubernetes (AKS, GKE, or EKS). Strong troubleshooting and root-cause analysis skills in distributed systems. Experience with observability platforms (e.g., DataDog, Prometheus/Grafana, OpenTelemetry). Ability to define and implement metrics, dashboards, and alerting. Demonstrated ability to work autonomously and own technical outcomes. Strong understanding of cloud Infrastructure and Networking architectures and automation. Nice to haves: Experience supporting regulated environments (healthcare, biotech, financial). Familiarity with compliance-driven change management and release processes (FDA, HIPAA). Knowledge of CI/CD deployment strategies and change automation. Experience with both GCP and Azure cloud platforms. Interest in mentorship and system reliability practices at scale. Benefits and additional information: The US target range of our base salary for new hires is $131,325 - $201,000. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-REMOTE

About this opportunity: At Freenome, we are seeking a Contract Clinical Research Associate to help grow the Freenome Clinical Development team. The ideal candidate is well-organized, an excellent communicator and experienced in supporting clinical trial execution for diagnostics products. This person is responsible for all things related to assigned aspects of clinical trial start-up and study progress including documentation collection and tracking. You are passionate about clinical research, attention to detail and Good Clinical Practice, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Director of Clinical Operations. This role will be a Remote role with occasional travel, as required, to our Brisbane, California headquarters. What you'll do: Coordinate and assist with trial start-up activities, including budget and contract negotiations, ICF revisions, and essential document packages Coordinate and track study documentation and other functional activities that relate to the conduct of clinical trials Facilitate resolution of laboratory queries Track metrics and study start-up timelines to identify trends and opportunities for improvement Track and report on study progress, including site activation, patient enrollment, monitoring visits Ensure that all essential study documents are filed appropriately and kept in an organized central repository for the project team (Veeva Vault) Lead the management of the TMF, including establishing QC processes and reconciliation of findings Assist with protocol and study-specific training with vendors, site personnel, and clinical sites Support Clinical Trial Managers and Clinical Research Associates with vendor management activities Must haves: Minimum Bachelor's degree in a life science-related field 2+ years' experience in a clinical trials research environment required, as a Clinical Trial Coordinator or Clinical Trial Assistant General knowledge of regulatory requirements & GCP Ability to multi-task, deal with shifting priorities, and proactively solve problems/manage risks Proficient in Microsoft Office or Google Suite Strong interpersonal, collaborative, and time management abilities Excellent attention to detail and the ability to keep detailed, accurate records High proficiency in Veeva Vault CTMS and eTMF systems Strong spoken and written communication skills Nice to haves: Previous experience in the cancer early detection or diagnostics space Additional information: Contractors may be hired through a third-party provider and will be considered contingent workers. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-REMOTE

About this opportunity: Freenome is hiring a Systems Integration Engineer to participate in a cross-functional team and contribute to the development of next generation NGS assays/products for early cancer detection. You will work in a Product Development team of world-class Scientists and Engineers focused on delivering Freenome's IVD assay portfolio. If you are passionate about deploying the power of NGS-based diagnostics in clinical care, and take pride in providing technical expertise to a growing team of Systems Integration Engineers, making a significant individual impact, we would love to speak with you! As part of a dynamic, flexible company you will be adapting to rapid technological progress and change, and help the team building the platform do the same. The role reports to the Senior Manager, Development & Scientific Operations. This role will be an onsite role based in our Brisbane, California headquarters. What you'll do: Execute end-to-end assay workflows using industry-leading automation platforms to support development of Freenome's next generation diagnostic products. Hands-on design and execution of complex test methods to assess hardware and system performance per Design Input Requirements. Evaluate resulting system performance, speed and throughput, and identify root causes for system-level issues and failures. Contribute to dFMEA, pFMEA, risk management, hazard assessment, and design review sessions with Engineering, Automation, and Systems Integration teams. Analyze outputs and identify HW, FW, and SW mitigating solutions to implement adequate risk control measures. Identify and steward Systems Integration initiatives to enable achievement of critical path project milestones/timelines. Support the system evaluation process through development and execution of system level test plans and protocols, including data analysis, interpretation and communication of results and their impact through written reports, design reviews, and interactive discussions. Apply sophisticated analytical problem solving skills to reagent and system integration issues to identify critical performance factors for assay development. Apply broad scientific, technical or professional concepts in accordance with area(s) objectives. Assess results for applicability, validity, and conformance to Product Requirements. Write and manage requirements as part of Project Team. Create and maintain design documentation in Design History Files. Must haves: Bachelor's degree or Master's degree with 2+ years of relevant work experience OR Doctoral degree. Education or equivalent experience in a relevant field such as Biology, Biochemistry, Bioengineering, Biomedical Engineering, etc. Previous experience as a hands-on engineer, scientist, or product developer (e.g. System Integration Scientist / Engineer, System Development Scientist / Engineer, or related occupation). Experience with developing and integrating complex instrumentation systems which incorporate optical, mechanical, thermal, and firmware components. Data analysis expertise and experience with various data analysis software packages. Well-developed mathematical and statistical analysis skills. (i.e., JMP, R, DOE). Knowledge of SQL, Python, R or other programming languages highly desired. Knowledge of a broad range of principles of biology, chemistry and physics, such as spectroscopic techniques, organic chemistry, electromagnetic theory, and thermodynamics. Strong integration analytical, process validation and troubleshooting skills to understand system interfaces and be able to quickly analyze, troubleshoot, and resolve system interoperability problems. Working knowledge of design of experiments, interpretation of test results, failure investigation and root cause failure analysis. Excellent communication skills, verbal and written. Demonstrated ability to understand and comply with applicable FDA regulations and company operating procedures, processes, policies and tasks. Work as part of a team to guarantee high quality of technical and design control documentation in alignment with Freenome's Quality requirements. Benefits and additional information: The US target range of our base salary for new hires is $100,725 - $140,700. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: The Technical Product Manager III (Clinical Interfaces) will be responsible for planning and coordinating the execution of Freenome's engineering initiatives for test ordering, blood collection and processing, and test reporting. You will create, plan, and execute software development plans while ensuring usability, scalability, and efficiency for our customers as well as the clinical laboratory and client services teams. You will gather requirements from end users and stakeholders, determine workflow solutions, and prioritize technical development in alignment with cross-functional teams, ensuring seamless customer experience. This role will empower you to spearhead discussions with key-decision makers and teams to create a comprehensive software roadmap outlining Freenome's path to commercialization and ongoing product development. Attention to detail will be paramount in this heavily regulated field and new software ecosystem. You will work closely with our engineering and IT teams, leveraging your deep knowledge in Agile methodologies (Scrum, Kanban, sprint planning, etc). The role reports to the Associate Director, Technical Product Management. This role will be a remote role, with onsite travel to our headquarters in Brisbane, California as needed. What you'll do: Manage the development of software systems, processes, and infrastructure to support order to cash processes Partner with lab and business stakeholders to elucidate requirements, optimize workflows, and lead product definition, ensuring alignment with regulatory standards (e.g., FDA or CE-mark). Work with engineers to translate product requirements into Epics and Stories with clear user acceptance criteria. Track and drive development and ensure fulfillment of requirements using issue tracking system (e.g., Jira). Lead and facilitate productive interactions between users and engineers to ensure user needs are understood and met. Create a thorough technical strategy and roadmap to scale Freenome's software systems to support current and future products Provide a clear and tangible vision for future development efforts with scalability in mind. Ensure seamless customer experience with technical and process-oriented solutions. Must haves: Bachelor's degree in an analytical, technical, or scientific field; advanced degree preferred. At least 5 years of experience in a software development environment, ideally with order-to-cash processes and operations for a clinical laboratory. Deep expertise in identification and prioritization of software features. Demonstrated ability to successfully lead complex trade-off decisions between functions and measurably improve organizational success and processes. Experience leading software development efforts to meet regulated market standards (e.g., FDA or CE-mark), laboratory operations, medical affairs, or clinical study operations for diagnostics a plus. Benefits and additional information: The US target range of our base salary for new hires is $118,150 - $167,475. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-REMOTE

About this opportunity: At Freenome, we are seeking a Senior Machine Learning Scientist to help grow the Machine Learning Science team, within the Computational Science department. The ideal candidate has a strong knowledge of artificial intelligence (AI), including machine learning (ML) fundamentals and extensive experience with deep learning (DL) methods, a track record of successfully using these methods to answer complex research questions, and the ability to thrive in a highly cross-functional environment. They will be responsible for the development of algorithms for early, blood-based detection tests for cancer. They will build on a foundation of ML/DL and statistical skills to develop models for identifying molecular signals from blood. They will also work with computational biologists, molecular biologists and ML engineers to design and drive research experiments, and will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Director, Machine Learning Science. This role can be a Hybrid role based in our Brisbane, California headquarters (2-3 days per week in office), or remote. What you'll do: Independently pursue cutting edge research in AI applied to biological problems (including cancer research, genomics, computational biology, immunology, etc.). Build new models or fine-tune existing models to identify biological changes resulting from disease. Build models that achieve high accuracy and that generalize robustly to new data. Apply contemporary interpretability techniques to provide a deeper understanding of the underlying signal identified by the model, ideally suggesting potential biological mechanisms. Work closely with ML Engineering partners to ensure that Freenome's computational infrastructure supports optimal model training and iteration. Take a mindful, transparent, and humane approach to your work. Must haves: PhD or equivalent research experience with an AI emphasis and in a relevant, quantitative field such as Computer Science, Statistics, Mathematics, Engineering, Computational Biology, or Bioinformatics. 3+ years of postdoc or post-PhD industry experience achieving impactful results using relevant modeling techniques. Expertise, demonstrated by research publications or industry achievements, in applied machine learning, deep learning and complex data modeling. Practical and theoretical understanding of fundamental ML models like generalized linear models, kernel machines, decision trees and forests, neural networks. Practical and theoretical understanding of DL models like large language models or other foundation models. Extensive experience with training paradigms like supervised learning, self-supervised learning, and contrastive learning. Proficient in current state of the art in ML/DL approaches in different domains, with an ability to envision their applications in biological data. Proficiency in a general-purpose programming language: Python, R, Java, C, C++, etc. Proficiency in one or more ML frameworks such as; Pytorch, Tensorflow and Jax; and ML platforms like Hugging Face. Experience in ML analysis and developer tools like TensorBoard, MLflow or Weights & Biases. Excellent ability to communicate across disciplines, work collaboratively, and make progress in smaller steps via experimental iterations. A passion for innovation and demonstrated initiative in tackling new areas of research. Nice to haves: Deep domain-specific experience in computational biology, genomics, proteomics or a related field. Experience in building DL models for genomic data, with knowledge of state-of-the-art DNA foundation models. Experience in NGS data analysis and bioinformatic pipelines. Experience with containerized cloud computing environments such as Docker in GCP, Azure, or AWS. Experience in a production software engineering environment, including the use of automated regression testing, version control, and deployment systems. Benefits and additional information: The US target range of our base salary/hourly rate for new hires is $173,775 - $246,750. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-HYBRID

About this opportunity: Freenome is seeking a hands-on, highly visible Corporate Controller who will be responsible for leading and coordinating the overall day-to-day activities of the accounting department. The Corporate Controller will play a crucial role in building scalable accounting processes to enable timely and accurate financial reporting, ensuring SOX compliance. This position will report directly to the Chief Financial Officer and the role is located in our Brisbane, CA headquarters. What you'll do: Accounting Close and Financial Reporting: Hands-on management of accounting close process with focused effort to continuously drive efficiencies in order to enable an accurate 5-day accounting close. Review and approve journal entries and account reconciliations as appropriate; enhance documentation and evidence of review over journal entries and account reconciliations to meet SOX compliance requirements. Implement balance sheet, income statement, and cash flow analytics as part of the accounting close process to support internal management reporting. Implement processes to identify and review accounting implications of non-standard contracts and agreements to ensure that appropriate technical accounting matters are documented and implemented in the Company's accounting records. Lead and drive the implementation/upgrade of various systems and leverage technology to build scalable/sustainable processes to create efficiencies in the accounting close and reporting processes (e.g., leverage power of NetSuite to build out reporting capabilities). Prepare and/or review schedules to support the preparation of external financial statements, footnotes, and MD&A (e.g., 10-Q, 10-K, S-1). Prepare and present materials at board and related committee meetings (e.g., audit committee); manage audit committee charter to ensure all mandated audit committee actions are addressed. Financial Operations: Develop and implement best-in-class procure to pay processes; evaluate, provide recommendations, and update financial approval matrix and workflows. Support the implementation of a Contract Lifecycle Management System. Oversee compliance with Travel & Entertainment (T&E) Policy and corporate credit card program; evaluate current T&E expense management reporting software and propose/implement alternative solutions. Oversee treasury process and external tax service providers. Internal Controls and Compliance: Collaborate closely with Director, SEC Reporting/SOX Compliance to ensure appropriate controls over financial processes are designed and operating effectively. Responsible for maintaining strong internal controls and ensuring accounting team is effectively trained. Coordinate quarterly reviews and annual audits with external auditors; ensure that all PBCs are prepared accurately and provided timely to support an efficient and unqualified audit; support internal audits and SOX audits as required. Stay updated on relevant accounting standards and regulatory changes impacting the biotech/diagnostic industry. Public Company Readiness: Maintain state of public company readiness, including operating under public company accounting close and reporting timelines, facilitating external auditor quarterly reviews, providing supporting schedules to Director, SEC Reporting/SOX. Compliance for preparation of quarterly footnotes and MD&A. Support due diligence efforts and interface with external stakeholders, including underwriters and legal counsel in connection with potential IPO diligence. Team Leadership and Development: Provide strong leadership and guidance to the accounting team, fostering a culture of excellence and continuous improvement. Promote professional development and skill enhancement initiatives to build a high-performing accounting organization. Collaborate cross-functionally with other departments to drive financial literacy and accountability throughout the organization. Must haves: Bachelor's degree in Accounting or related field (advanced degree preferred). Active Certified Public Accountant (CPA) license. Strong technical accounting skills and proficiency in implementation of U.S. GAAP, Sarbanes-Oxley, and SEC regulations. Minimum of 12+ years of relevant experience, including controllership roles in a publicly traded life science company. Minimum 8+ years of leadership experience building and cultivating high-performance accounting teams. Biotechnology/pharmaceutical/diagnostic industry experience required; experience building out accounting operations for a commercial organization are highly desirable. Must have experience implementing and managing a global legal entity structure in NetSuite. Strong customer-focus and the demonstrated ability to build new capabilities with a process-oriented mindset. Results-driven with a high sense of urgency, ownership, and proven ability to meet tight timelines and manage competing priorities in a dynamic environment. Exceptional communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams, Freenome's leadership, and external stakeholders. Proven leadership and team-building skills, with the ability to motivate others towards achieving common goals. Nice to haves: Experience at a Big 4 public accounting firm. Benefits and additional information: The US target range of our base salary for new hires is $223,125 - $319,200. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-HYBRID

About this opportunity: At Freenome, we are seeking a Research Associate II to help grow the Freenome Genomics Late Stage Development team. The ideal candidate is highly analytical and detail-oriented, with a strong foundation in molecular biology and knowledge of next-generation sequencing (NGS) technologies. This person is responsible for all things related to developing and validating clinical-grade assays to measure complex, blood-based analytes (e.g., whole-genome sequencing of cf DNA). You are passionate about advancing cancer diagnostics, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Manager of Genomics Late Stage Development. This role will be an onsite role based in our Brisbane, California headquarters. What you'll do: Apply knowledge of molecular biology, nucleic-acid biochemistry, and next-generation sequencing to develop assays for DNA, including genome-wide and targeted approaches. Characterize automated assays by generating and analyzing experimental data. Create and manipulate high impact assay inputs, including samples and reagents formulation as required. Gather high-quality data, take detailed notes, and openly communicate on lessons learned while performing experiments. Collaborate with development team and computational biologists, analyze data and generate study conclusions. Collaborate with clinical laboratory members to transition development protocols into production, including automation, validation experiments, and SOP development. Present data in cross functional teams. Contribute to study protocols and reports. Must haves: Bachelors with 2+ years of relevant industry experience or Masters in molecular biology, or a related field. Hands-on experience in NGS based assay development including sample preparation, library preparation, target capture, and sequencing. Experience with automated platforms in plate-based, low-volume formats and/or microfluidics and experience working with automated liquid handlers. Biological understanding of human cell-free nucleic acids and/or cancer biology. High attention to detail and ability to record accurate and detailed observations, assess impact, and perform troubleshooting as required. Flexible and highly motivated to learn new skills and comfortable adapting to changing priorities. Ability to manual pipette with high confidence, accuracy, and precision. Clear and proactive communication skills and ability to collaborate effectively with team members in the same and adjacent disciplines. Nice to haves: Experience working in a regulated laboratory environment (CLIA, GLP/GCLP, IVD development). Experience using ELN (electronic lab notebook) and LIMS (lab information management system). Familiarity with programing in a scientific programming language (e.g., Python or R). Benefits and additional information: The US target range of our hourly rate for new hires is $37.68 - $51.92. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: At Freenome, we are seeking a motivated Lab Technician to help grow the Freenome Scientific Operations team. The ideal candidate is eager to learn and able to work with urgency in an ever changing environment. This person is responsible for all things related to R&D support - reagents, equipment, consumables, study support. You are passionate about fighting cancer, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Supervisor, R&D Labs. This role will be an Onsite role. What you'll do: Collaborate with the Research, Development, Automation, Facilities and Supply Chain teams to ensure consistent laboratory support Assist Research Associates and Scientists in preparing and aliquoting reagents Perform routine maintenance on a variety of laboratory equipment Assist with troubleshooting R&D lab equipment issues using established SOPs and WI's Operate automated liquid handling platforms to execute automated procedures Assist with monitoring cold storage temperatures and respond to temperature excursion events Assist with organizing and maintaining R&D reagent and sample inventory documentation Act as a role model by demonstrating adherence to all proper safety protocols Perform Accessioning and processing of patient samples Support Biosample Management by picking and pulling samples Contribute to Study Execution by performing Genomics workflows Must haves: Bachelor's Degree with 1-2 years of related experience Strong communication skills and the ability to collaborate across disciplines Experience in writing or updating documentation such as WI's, SOPs and maintaining a detailed Lab notebook Ability to follow SOPs and troubleshoot effectively Strong understanding of current molecular biology techniques and DNA sequencing Attention to detail and documentation practices within a repetitive work function Nice to haves: Valuable supplementary skills include: Experience handling and preparing blood and tissue samples Proficiency with automated liquid handling platforms and software Experience setting up Illumina sequencers Experience maintaining laboratory equipment Experience writing or updating documentation such as work instructions and SOPs Experience working in BSL-2 laboratories and familiarity with 5S organizational practices Benefits and additional information: The US target range of our hourly rate for new hires is $30.60 - $42.07. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE

About this opportunity: At Freenome, we are seeking a contract Clinical Research Associate to help grow the Freenome Clinical Development team. The ideal candidate is well-organized, an excellent communicator and experienced in diagnostics clinical trial management. This person is responsible for all things related to assigned aspects of clinical trial monitoring and site management. You are passionate about clinical research, attention to detail and Good Clinical Practice, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Director of Clinical Operations. This role will be a remote role with occasional travel, as required, to our Brisbane, California headquarters. What you'll do: * Ensure compliance with standard protocol and regulatory and ICH GCP obligations in assigned aspects of clinical site monitoring, such as site initiation, routine monitoring, maintenance of study files, study close out, and retrieval of study materials * Complete on-site and remote monitoring activities in compliance with the Clinical Monitoring Plan, including source document verification for accuracy and integrity, as required * Write and submit reports of investigational site findings and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate Must haves: * Minimum Bachelor's degree in a life science-related field, a registered nurse (RN) certification, or equivalent * 3+ years' experience in a clinical trials research environment required, with specific in vitro diagnostics study experience * General knowledge of regulatory requirements & GCP * Ability to multi-task, deal with shifting priorities, and proactively solve problems/manage risks * Strong interpersonal, collaborative, and time management abilities * Excellent organizational skills; accurate and detail-oriented * High proficiency in Veeva Vault and Medrio * Strong spoken and written communication skills Nice to haves: * CRA certification by recognized professional organization is a plus, but not mandatory * Previous experience in the cancer early detection space Additional information: Contractors may be hired through a third-party provider and will be considered contingent workers. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. * Family & Medical Leave Act (FMLA) * Equal Employment Opportunity (EEO) * Employee Polygraph Protection Act (EPPA) #LI-REMOTE

About this opportunity: Our infrastructure team is a small but critical group where you will help set the culture and build the systems that allow us to move fast without breaking things. This is an opportunity to do meaningful engineering work that will directly save lives. We value: Rapid iteration and tight feedback loops. Continual improvement rather than disruption. Technical simplicity and elegance. A focus on the larger goals. Mutual respect and blameless postmortems. A culture of diversity and inclusion. As a Senior Software Engineer, you will help design, build, and maintain secure and scalable infrastructure across our cloud environments. You'll contribute to projects that support our clinical lab systems, scientific computing pipelines, and regulated production workloads - while growing your technical leadership and deepening your infrastructure expertise. This role is ideal for an engineer who is experienced with cloud platforms and Kubernetes, comfortable working independently, and ready to take ownership of well-scoped systems or infrastructure components. Additionally, this role is Hybrid and will entail managing our onsite Nvidia infrastructure. As an engineering-forward biotech company, we apply modern engineering practices to build reliable, maintainable, scalable, and secure production systems for our clinical lab and Computational and Molecular Research Scientists. The role reports to the Director, Cloud Infrastructure. What you'll do: Execution: Design and implement cloud infrastructure components using Pulumi (Python). Manage and maintain Kubernetes clusters (AKS, GKE), including node pools, ILBs, and autoscaling configurations. Define observability patterns and implement metrics, dashboards, and alerts in support of production reliability. Contribute to our CI/CD platforms, including build pipeline improvements, deployment strategies, and release automation. Participate in incident response and postmortem analysis for infrastructure-related outages or events. Communication and Collaboration: Partner with team members, TPMs, and security stakeholders to deliver infrastructure that meets compliance and reliability requirements. Lead technical implementation of projects or initiatives within your scope. Perform thorough, constructive code reviews and help level up peers through pairing and design discussions. Communicate clearly with cross-functional teams and represent infrastructure in collaborative settings. Culture: Model Freenome's values and principles in your work and interactions. Promote a collaborative, respectful engineering culture with clear communication and inclusive practices. Actively contribute to documentation, playbooks, and engineering standards within the team. Help foster a strong team culture of accountability, learning, and psychological safety. Technical Leadership: Independently lead the delivery of projects or well-bounded infrastructure systems. Provide mentorship to junior engineers and review designs within your domain. Know when to make architectural tradeoffs with guidance and justify design decisions based on long-term impact. Help evolve our infrastructure practices and participate in team strategy discussions. Must haves: Bachelor's degree in Computer Science, Engineering, or equivalent work experience. Experience with NVIDIA DGX systems and NVIDIA software tech stack. 5+ years of experience in software engineering roles (Python preferred), with at least 2 years focused on cloud infrastructure. Production experience with Kubernetes in cloud environments (e.g., AKS, GKE, or EKS). Proficiency with Terraform, Pulumi, or similar IaC tools. Experience with CI/CD, including deployment automation and release strategies. Familiarity with cloud IAM, networking, and security best practices. Strong troubleshooting and root cause analysis skills in distributed systems. Demonstrated ability to work autonomously and own technical outcomes. Nice to haves: Experience supporting infrastructure in regulated environments (e.g., healthcare, biotech, financial). Background in observability platforms such as Prometheus, Grafana, OpenTelemetry). Exposure to cost optimization, audit logging, or compliance automation in cloud platforms. Experience working with scientists, data engineers, or platform users in cross-functional settings. Interest in mentorship, system design, and infrastructure patterns at scale. Experience with Microsoft Azure. Benefits and additional information: The US target range of our base salary for new hires is $131,325 - $189,525. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-HYBRID

About this opportunity: At Freenome, we are seeking a Staff Machine Learning Scientist to help grow the Machine Learning Science team, within the Computational Science department. The ideal candidate has a strong knowledge of artificial intelligence (AI), including machine learning (ML) fundamentals and extensive experience with deep learning (DL) methods, a track record of successfully using these methods to answer complex research questions, the ability to drive independent research and thrive in a highly cross-functional environment. They will be responsible for the development of algorithms for early, blood-based detection tests for cancer. They will build on a foundation of ML/DL and statistical skills to develop models for identifying molecular signals from blood. They will also work with computational biologists, molecular biologists and ML engineers to design and drive research experiments, and will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Director, Machine Learning Science. This role can be a Hybrid role based in our Brisbane, California headquarters (2-3 days per week in office), or remote. What you'll do: Independently pursue cutting edge research in AI applied to biological problems (including cancer research, genomics, computational biology, immunology, etc.). Build new models or fine-tune existing models to identify biological changes resulting from disease. Build models that achieve high accuracy and that generalize robustly to new data. Apply contemporary interpretability techniques to provide a deeper understanding of the underlying signal identified by the model, ideally suggesting potential biological mechanisms. Work closely with ML Engineering partners to ensure that Freenome's computational infrastructure supports optimal model training and iteration. Take a mindful, transparent, and humane approach to your work. Must haves: PhD or equivalent research experience with an AI emphasis and in a relevant, quantitative field such as Computer Science, Statistics, Mathematics, Engineering, Computational Biology, or Bioinformatics. 6+ years of postdoc or post-PhD industry experience achieving impactful results using relevant modeling techniques. Expertise demonstrated by research publications or industry achievements, in driving independent research in applied machine learning, deep learning and complex data modeling. Practical and theoretical understanding of fundamental ML models like generalized linear models, kernel machines, decision trees and forests, neural networks, boosting and model aggregation. Practical and theoretical understanding of DL models like large language models or other foundation models. Extensive experience with training paradigms like supervised learning, self-supervised learning, and contrastive learning. Proficient in current state of the art in ML/DL approaches in different domains, with an ability to envision their applications in biological data. Proficiency in a general-purpose programming language: Python, R, Java, C, C++, etc. Proficiency in one or more ML frameworks such as; Pytorch, Tensorflow and Jax; and ML platforms like Hugging Face. Experience in ML analysis and developer tools like TensorBoard, MLflow or Weights & Biases. Excellent ability to communicate across disciplines, work collaboratively, and make progress in smaller steps via experimental iterations. Proficient at productive cross-functional scientific communication and collaboration with software engineers and computational biologists. A passion for innovation and demonstrated initiative in tackling new areas of research. Nice to haves: Deep domain-specific experience in computational biology, genomics, proteomics or a related field. Experience in building DL models for genomic data, with knowledge of state-of-the-art DNA foundation models. Experience in NGS data analysis and bioinformatic pipelines. Experience with containerized cloud computing environments such as Docker in GCP, Azure, or AWS. Experience in a production software engineering environment, including the use of automated regression testing, version control, and deployment systems. Benefits and additional information: The US target range of our base salary for new hires is $199,675.00 - $283,500.00. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-HYBRID

About this opportunity: Freenome is looking for a Vice President, Market Access as a key member of our rapidly developing Commercial team. The ideal candidate will have hands-on experience in Market Access & Reimbursement for an in vitro diagnostic (IVD). In this role, you will be instrumental in crafting and executing market access strategies that will support launch and early commercialization for Freenome products. As a member of the extended leadership team (ELT), you will participate in guiding and refining company-level strategy. Your commitment to patient care and access will significantly contribute to our growth and our mission to outpace cancer with early detection. This role will report to the Chief Commercial Officer and will serve as a vital part of the Commercial leadership team. This is a remote role with the requirement to travel up to 30% of the time. What you'll do: Market Access & Pricing Spearhead the development and execution of market access strategies to enhance patient access, secure reimbursement, and encourage product adoption. Lead coding, coverage, and pricing initiatives to ensure reimbursement for our CRC screening test upon FDA approval and future product pipeline. Craft access, reimbursement, and contracting strategies for various payer segments and geographies, aligning with our go-to-market roadmap. Perform pricing analysis and modeling to establish optimal pricing and contracting that maximizes patient access and revenue. Identify and build out the appropriate team to support our market access goals. Collaborate with commercial, finance, and medical teams to develop value propositions, payer messaging, pricing strategies and evidence generation plans that support our market access goals. Offer strategic leadership on policy issues, access-related market dynamics, and reimbursement. Partner with Freenome's Revenue Cycle/Billing team to ensure the Average Selling Price (ASP) for each Freenome product is optimized through effective pricing strategies, payer negotiations, and claims and appeals management. External Engagement Monitor and report on healthcare policies, regulations, and trends that affect market access. Engage with payers, government entities, and stakeholders to inform market access strategies. Influence healthcare policies and reimbursement practices through engagement with policymakers and advocacy groups. Conduct market research to understand the payer landscape and policy trends. Cross-Functional Launch Execution Lead market access launch readiness, including building out the necessary team to support our go-to-market plan. Work with internal stakeholders to ensure market access strategies are in sync with business goals. Develop KPIs to monitor the effectiveness of market access strategies. Collaborate with Marketing, Legal, and Regulatory Affairs to drive coordinated payer engagement. Must haves: Bachelor's degree. 15+ years of commercial experience in diagnostics, pharmaceuticals, or biotech; diagnostics experience required. 10+ years in Market Access with direct responsibility for pricing, reimbursement, or policy across the product lifecycle. Experience in cancer or preventative screening, primary care, oncology, and/or consumer sectors. In-depth knowledge of the healthcare ecosystem, including economics, policy, and the regulatory environment in the U.S. Familiarity with customer types such as HCPs, patients, payers, IDNs, and their business models. Proven track record in creating and executing access and reimbursement strategies. Ability to build pricing and reimbursement models for diagnostics. Knowledge of regulatory guidelines and compliance requirements. Highly collaborative with strong interpersonal skills and relationship-building capabilities. Entrepreneurial mindset with a proactive approach to problem-solving. Ability to craft and convey the company's story compellingly to various audiences. Nice to haves: SF Bay Area residency is a plus but not mandatory. An MBA is advantageous but not essential. Experience with pricing, coding and coverage for Advanced Diagnostic Laboratory Tests (ADLTs). Experience in IVD or laboratory developed test (LDT) market access. Experience in market research, analysis, or planning in the pharmaceutical, biotechnology, or related industry is beneficial. Experience leading a reimbursement and billing team is a plus. Benefits and additional information: The US target range of our base salary rate for new hires is $293,550 - $383,775. You will also be eligible to receive pre-IPO equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-REMOTE

About this opportunity: At Freenome, we are seeking a Research Associate II to join our Reagent Development team within Genomic Early Development. As a Research Associate II, you will participate in the development of genomic assay technologies and contribute to Freenome's multiomic product portfolio aimed at early cancer detection. You will work closely with Scientists, Automation Engineers, and Computational Biologists to develop, optimize, and characterize efficient automated workflows to improve experimental and clinical throughput in a regulated high throughput environment. You will also work with Operations, Quality, and Regulatory to transfer complex methodologies, processes, and assays to Operations to ensure the highest quality data is produced by our clinical lab. You are passionate about contributing to developing life-saving diagnostics through early cancer detection, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. The role reports to the Senior Manager of Genomic Early Development team. This role will be an onsite role based in Brisbane, California headquarters. What you'll do: Apply hands-on knowledge of molecular biology, nucleic-acid biochemistry and next generation sequencing to develop and optimize NGS based methods and processes following principles of Design Controls for IVD development. Design and perform experiments to develop and optimize NGS workflow including DNA/RNA extraction, library preparation, target capture, and sequencing. Operate and maintain NGS related instruments such as automated liquid handlers, PCR instruments, and sequencers. Conduct new reagents testing and develop reagent quality control methods. Participate in troubleshooting issues, identify and implement process improvement for the entire analytical workflow. Collaborate with research, computational scientists, and automation engineers to transfer research prototype assays from Research to Development. Collaborate with Quality Control Lab, Manufacturing lab, Quality, and Regulatory to transfer reagent quality control methods and manufacturing processes from Development to Operations and support the implementation of the methods and processes in Operations. Accurately record results in electronic lab notebooks, author work instructions and record forms, contribute to writing study protocols and reports. Diligently apply current Good Laboratory and Documentation Practices (cGLP, cGDP). Exemplify Freenome cultural values across the organization. Must haves: Bachelor's in molecular biology, biochemistry, or a related field with 2+ years of experience in the life sciences or Master's in molecular biology or a related field. Hands-on experience in Next-gen sequencing (NGS) based automated assay development including extraction, library preparation, target capture, and sequencing. Hands-on experience in nucleic acid preparation, amplification, and quantification (DNA/RNA extraction and purification, PCR, qPCR, dd PCR, Qubit, Fragment Analyzer, Tapestation). Experience in working with ct DNA/cf DNA as an analyte in NGS workflows. Experience with automated platforms in plate-based, low-volume formats and experience working with automated liquid handlers. High attention to detail and ability to record accurate and detailed observations, assess impact, and perform troubleshooting as required. Ability to perform data analysis and to be critical of results obtained during experimentation. Clear and proactive communication skills and ability to collaborate effectively with team members in the same and adjacent disciplines. Nice to haves: Experience working in a regulated laboratory environment (CLIA, GLP/GCLP, IVD development) strongly desired. Experience in programing in a scientific programming language (e.g., Python or R). Benefits and additional information: The US target range of our hourly rate for new hires is $37.68 - $51.92. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information. Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Applicants have rights under Federal Employment Laws. Family & Medical Leave Act (FMLA) Equal Employment Opportunity (EEO) Employee Polygraph Protection Act (EPPA) #LI-ONSITE