Technical Product Manager III
FreenomeThis Product Manager role focuses on the Commercial Data Platform and data products within a biotechnology environment. You will manage technical roadmaps, infrastructure, and engineering workflows to support R&D and commercial operations.
What you’d own
- Commercial Data Platform roadmap and strategy
- Data pipelines and tooling development
- Translating requirements into Epics and Stories
- Ensuring data integrity and regulatory compliance (HIPAA, HITECH)
Who it’s for
A fit if you…
- ✓You have 5+ years of experience in software development environments.
- ✓You have a background in biotechnology, NGS, or clinical operations.
- ✓You are proficient in Agile methodologies like Scrum and Kanban.
- ✓You can navigate complex trade-offs between technical requirements and business needs.
Not for you if…
- ✗You prefer general consumer products over regulated medical/biotech data.
- ✗You prefer a role without heavy emphasis on technical infrastructure and pipelines.
- ✗You are looking for a non-technical product management track.
Reading between the lines
- The mention of 'regulatory standards' (FDA, CAP/CLIA) implies a high-stakes environment where documentation and compliance are as critical as the features themselves.
- Requirement to 'elucidate requirements' from lab stakeholders suggests you will need to translate complex scientific needs into actionable engineering tasks.
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Benefits
Full job description
About this opportunity: At Freenome, we are seeking a Technical Product Manager to join the Freenome Product Management team. This role will be responsible for planning and coordinating the execution of Freenome’s engineering initiatives for the Commercial Data Platform and Data Products. You will create, plan and execute software development plans while ensuring efficiency, scalability and usability for our Commercial, Laboratory, and R D teams.
You will gather requirements and prioritize technical development in alignment with cross-functional teams and stakeholders. This role will lead discussions with key-decision makers and stakeholders to create a comprehensive data platform roadmap outlining Freenome’s path to commercialization and support for ongoing product development. You will work closely with our engineering team, leveraging your deep knowledge in Agile methodologies (Scrum, Kanban, sprint planning, etc) to enable seamless execution.
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: Define requirements and manage the development processes, systems, and software infrastructure for the data platform and tools supporting Commercial and R D initiatives. Partner with lab and business stakeholders to elucidate requirements, optimize workflows, and lead data platform and product definition, ensuring alignment with regulatory standards (e.g., HIPAA, HITECH).
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 and operationalize a comprehensive technical strategy and integrated roadmap for Freenome’s data products, pipelines, and tooling while aligning cross-functional milestones and deliverables across current and future programs.
Provide a clear and tangible vision for future development efforts with scalability and accessibility in mind. Ensure complete data integrity throughout the pipeline 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 within biotechnology and NGS. 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 (FDA, CAP/CLIA), laboratory operations, medical affairs, or clinical study operations for diagnostics. Nice to haves: Experience in building solutions with a focus on multiomics, NGS, or proteomics 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) California applicants please review the CCPA Notice at Collection here: California Consumer Privacy Act (CCPA) #LI-REMOTE
About Freenome
See all roles →Freenome develops blood tests that detect cancer early, combining multiomics and machine learning with the convenience of a standard blood draw. Founded in 2014, it runs a large clinical program to validate its screening tests and has a commercialization partnership with Roche for markets outside the US. The company went public on Nasdaq in July 2026 through a SPAC merger. Its stated values are servant leadership, trust, integrity, and empathy, and it grants equity to every full-time US employee. For a PM, the draw is a regulated, science-heavy product where clinical, data, and business teams work closely together.
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