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Tech Stack
Tools & technologiesPMP
About the role
Key responsibilities & impact- Lead cross-functional programs supporting product development initiatives at the Boulder, CO site.
- Drive end-to-end execution of product development programs, including planning, scheduling, resource coordination, and risk management across assay, software, and systems development.
- Support regulatory product development activities, ensuring alignment with regulated processes and quality systems.
- Coordinate regulatory submission readiness, including support for Investigational Device Exemptions (IDEs), pre-submissions, and other global regulatory filings.
- Lead cross-functional alignment across R&D, software, regulatory, quality, and clinical teams to ensure clear requirements, priorities, and deliverables.
- Translate product strategy into actionable program roadmaps, including timelines, milestones, and interdependencies.
- Partner with Alliance Management to manage external biopharma and CDx partnerships, coordinating joint program plans, deliverables, timelines, and communication across organizations.
- Identify, track and manage program risks and dependencies.
- 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.
Requirements
What you’ll need- 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).
- 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.
- Strong organizational and program management skills, with the ability to manage multiple concurrent initiatives.
- Analytical mindset with strong attention to detail and ability to identify risks and dependencies.
- Excellent executive communication skills, with the ability to tailor messaging across technical and non-technical audiences.
- Proficiency with program management and collaboration tools (e.g., Smartsheets, JIRA, Office Timeline, etc.).
- Situational awareness, coupled with facilitation, problem solving, and conflict resolution skills to drive cross-functional decision-making.
Benefits
Comp & perks- Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
- Free testing for Natera employees and their immediate families.
- Fertility care benefits.
- Pregnancy and baby bonding leave.
- 401k benefits.
- Commuter benefits.
- Generous employee referral program.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
program managementproject managementproduct developmentregulatory submissionsdesign controlssoftware lifecycle processesNGS diagnosticsassay developmentrisk managementclinical trial operations
Soft Skills
organizational skillsanalytical mindsetattention to detailexecutive communicationproblem solvingconflict resolutionfacilitation skillscollaborative relationshipscross-functional alignmentability to manage multiple initiatives
Certifications
PMP