Senior Product Manager, Clinical Genomics

This is a fully remote position, open to applicants in United States.

📋 Description

• Establish and guide a multi-year product strategy and roadmap for one or more RIR components, ensuring alignment with clinical quality, regulatory standards, and commercial scalability goals.

• Collaborate with engineering leadership to shape platform-level technical direction.

• Work closely with software engineering, bioinformatics, clinical domain specialists, quality assurance, regulatory bodies, and other product teams.

• Convert business, clinical, and operational requirements into clear, actionable product specifications.

• Define and enhance comprehensive user workflows, incorporating UI/UX requirements along with necessary backend functionalities.

• Foster cross-team alignment on shared data contracts and workflow protocols.

• Mentor others and elevate product management standards within the RIR organization.

• Take ownership of measurable enhancements in clinical workflow efficiency, reliability, and operational scalability.

• Develop prioritization frameworks that balance regulatory risks, clinical impacts, technical scalability, and business outcomes across RIR investments.

• Create and monitor quantitative metrics related to usability, performance, reliability, and user adoption.

• Lead delivery teams with clear strategic objectives, ensuring requirements align with long-term platform aspirations, validation preparedness, and system interoperability.

• Proactively identify systemic risks, architectural limitations, and workflow inefficiencies that may hinder scalability or regulatory compliance, leading cross-functional efforts to address these issues.

• Collaborate with Quality and Regulatory leadership to shape validation strategies, risk classifications, traceability, and audit preparedness for RIR software systems.

• Develop clear, data-driven proposals and presentations to facilitate stakeholder alignment and decision-making.

• Serve as a subject matter expert for assigned components, assisting in design, testing, validation, rollout, and ongoing utilization.

⛳️ Requirements

• Bachelor’s degree in life sciences, engineering, computer science, statistics, or a related field.

• Over 5 years of experience in software product management, including oversight of complex, multi-team or platform-level projects.

• At least 5 years of experience working on production software within healthcare, clinical genomics, or other regulated life sciences sectors, demonstrating impact on validation, compliance, and system scalability.

• Proven experience in influencing engineering architecture and long-term technical investment strategies.

• Established ability to drive consensus across highly matrixed organizations without direct authority.

• History of effectively operating in ambiguous environments and defining product direction independently.

🏝️ Benefits

• Comprehensive medical, dental, vision, life, and disability insurance plans available for eligible employees and their dependents.

• Complimentary testing for Natera employees and their immediate family members.

• Fertility care benefits offered.

• Leave for pregnancy and baby bonding available.

• 401k retirement benefits provided.

• Commuter benefits are included.

• Generous employee referral program in place.