Natera
biotechnology, diagnostics, clinical laboratory, life sciences
ProgramManager
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“Program Manager at Natera. Skills: Program Management, Product Development, Regulated Environments, Cross-functional Leadership, Stakeholder Management. lead cross-functional programs supporting product development initiatives. driving execution across product development cross functional teams”
What You'll Achieve.
enable timely, informed decision-making; driving issue resolution; ensure alignment, ownership, and timely execution
Industry & Context.
problem solving; conflict resolution; Analytical mindset with attention to detail and ability to identify risks and dependencies
This position may be required to work across time zones as needed to support project schedules
What They're Looking For.
Must Have
3-5+ years of experience in program management, or equivalent combination of project management and relevant functional experience in biotechnology, diagnostics, clinical laboratory, or life sciences, Experience supporting product development in regulated environments (IVD, medical device, or similar)
Nice to Have
Background in NGS diagnostics, including assay and software components (MRD experience preferred), familiarity with design controls (ISO 13485) and software lifecycle processes (IEC 62304), Experience supporting regulatory submissions (e. g. , IDE, 510(k), PMA, or equivalent) preferred, Exposure to clinical trial operations and execution (preferred), Experience working with external partners, such as biopharma or CDx collaborations (preferred), PMP or equivalent certification preferred
What You'll Do.
lead cross-functional programs supporting product development initiatives
driving execution across product development cross functional teams
present data-driven recommendations and business proposals to senior leadership
track and manage program risks and dependencies
proactively identifying mitigation strategies and driving issue resolution
Drive cross-functional accountability
Support continuous improvement of product development processes
and cross-functional ways of working
build and maintain positive and collaborative relationships with cross-functional teams
How You'll Work.
Team & Collaboration
lead cross-functional programs; driving execution across product development cross functional teams; Drive cross-functional accountability; Cultivate, build and maintain positive and collaborative relationships with cross-functional teams; Ability to influence senior stakeholders and drive alignment in matrixed organizations; Inclusive collaboration
Communication Scope
Excellent executive communication skills; ability to tailor messaging across technical and non-technical audiences
Process & Methodology
program management, project management, manage multiple concurrent initiatives, identify risks and dependencies, facilitation, problem solving, conflict resolution
Full Job Description
POSITION SUMMARY: The Program Manager will lead cross-functional programs supporting product development initiatives at the Boulder, CO site. Projects and programs may include development, validation, and regulatory submission of diagnostic products; support of biopharma companion diagnostic (CDx) partnerships; and product sustainment and lifecycle management efforts. This role is responsible for driving execution across product development cross functional teams, including R escalate issues as needed; and present data-driven recommendations and business proposals to senior leadership to enable timely, informed decision-making. Identify, track and manage program risks and dependencies, proactively identifying mitigation strategies and driving issue resolution. Drive cross-functional accountability, influencing without direct authority to ensure alignment, ownership, and timely execution. Support continuous improvement of product development processes, tools, and cross-functional ways of working. Cultivate, build and maintain positive and collaborative relationships with cross-functional teams. QUALIFICATIONS: 3-5+ years of experience in program management, or equivalent combination of project management and relevant functional experience in biotechnology, diagnostics, clinical laboratory, or life sciences. Experience supporting product development in regulated environments (IVD, medical device, or similar). KNOWLEDGE, SKILLS, AND ABILITIES: Background in NGS diagnostics, including assay and software components (MRD experience preferred). Strong familiarity with design controls (ISO 13485) and software lifecycle processes (IEC 62304). Experience supporting regulatory submissions (e.g., IDE, 510(k), PMA, or equivalent) preferred. Exposure to clinical trial operations and execution (preferred). Experience working with external partners, such as biopharma or CDx collaborations (preferred). PMP or equivalent certification preferred. Ability to influence senior stakeholde
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