Natera · 3 hours ago
Strategic Program Manager
United States
Full-time
Remote
Mid Level
$107K/yr - $134K/yr
3+ years expNatera is a global leader in cell-free DNA testing, dedicated to oncology, women’s health, and organ health. They are seeking a Strategic Program Manager to lead cross-functional programs that drive the launch of new clinical diagnostic products and enhance existing ones, ensuring compliance with quality and regulatory standards.
BiotechnologyGeneticsHealth DiagnosticsMedicalWomen's
Responsibilities
Drive cross-functional programs that bring new clinical products to market and enhance existing ones, with a strong focus on Design Control and New Product Introduction in a regulated environment
Partner across teams—including R&D, business, operations, and engineering—to define goals, milestones, and plans that balance resources, risks, and priorities
Lead all phases of product development, from early concept through commercialization and post-launch, ensuring alignment, transparency, and momentum
Develop and maintain key program documentation, such as project plans, protocols, and reports, to keep teams informed and accountable
Track progress and communicate results through clear, data-driven reports and regular updates to senior leadership
Champion Design Control excellence, managing gate reviews, design freezes, technical assessments, change control, and regulatory deliverables
Facilitate productive team meetings that drive decisions, surface and mitigate risks, and maintain focus on program objectives
Guide trade-off and risk decisions to balance technical, business, and regulatory considerations and challenge assumptions while adapting to evolving priorities
Foster collaboration and problem-solving, helping teams overcome challenges, resolve conflicts, and deliver high-quality results on time
Coordinate joint development efforts with external partners to ensure seamless integration and progress
Manage up to 3 dynamic programs simultaneously, anticipating challenges and maintaining progress in a fast-paced environment
Qualification
Required
Bachelor's degree in Biology, Molecular Biology, Biochemistry, Bioinformatics, Computer Science, or a related technical discipline (or equivalent experience) required
Minimum 3 years of program management experience in biotech, life sciences, or another regulated technical industry
Proven experience creating and maintaining complex Gantt charts, project plans, and risk/RAID logs
Skilled proficiency with project management and scheduling tools such as SmartSheet (or equivalent)
Exceptional communication and interpersonal skills, with the ability to influence and collaborate effectively across technical and non-technical teams, including functional management
Highly organized, resilient and adaptable, with strong time-management and multitasking abilities in a fast-paced, evolving environment
Demonstrated ability to work independently while contributing effectively to cross-functional teams
Preferred
Master's degree or higher preferred
Project management certification or training (e.g., PMP or equivalent) preferred
Background in research, assay development, systems engineering, lab operations, or software development is highly desirable
Familiarity with laboratory informatics systems and processes such as LIMS, sample accessioning, sequencing pipelines, and results reporting preferred
Minimum 3 years of project budget management experience preferred
Experience with software development lifecycle principles, data architecture patterns (e.g., SOA), and agile tools (e.g., Jira, GitLab) a plus
Understanding of product development under FDA Design Controls, including documentation standards and relevant regulations (e.g., 21 CFR, ISO 13485, ISO 15189, EU IVDR and Section 524B for Cybersecurity) desirable
Benefits
Annual performance incentive bonus
Long-term equity awards
Comprehensive health benefits (medical, dental, vision)
401(k) with company match
Generous paid time off and company holidays
Additional wellness and work-life benefits
Commuter benefits
Pregnancy and baby bonding leave
Company
Natera
Natera specializes in cell-free DNA testing to provide a more targeted interventions to oncology, women's health, and organ health.
5001-10000 employees
H1B Sponsorship
Natera has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (90)
2024 (72)
2023 (37)
2022 (71)
2021 (64)
2020 (40)
Funding
Current Stage
Public CompanyTotal Funding
$1.16BKey Investors
Sofinnova InvestmentsLightspeed Venture PartnersSequoia Capital
2023-09-07Post Ipo Equity· $250M
2022-11-15Post Ipo Equity· $400.05M
2022-03-16Post Ipo Equity· $5M
Leadership Team
Steve Chapman
CEO
Jonathan Sheena
Co-Founder, Board Member
Recent News
2026-01-13
2026-01-13
Company data provided by crunchbase