Senior Program Manager
Natera · US Remote
Posted about 2 months ago · $119,000.00 - $148,700.00 · Previously reposted
or apply directly on Natera's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 55 days Natera's roles stay open a median of 55 days
- Reposted
- Yes taken down and listed again at least once
- Salary listed
- Yes 3% of Natera's roles list one
- Ghost-job risk at Natera
- high 143 stale, 24 reposted of 220 open
- Hiring momentum
- 377 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-27
Measured from postings appearing on and disappearing from Natera's own greenhouse board since 2026-08-03. Full hiring picture for Natera.
About this role
The Senior Program Manager will lead complex product development programs in the diagnostics and medical device space, overseeing projects from early development through clinical trials and regulatory submissions. This role involves collaboration with cross-functional teams, managing risks, and ensuring adherence to regulatory standards while also contributing to key deliverables such as design plans and documentation.
- benefits
- 4/5
- freshness
- 1/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Natera as an employer.
What you need
- 5-7+ years of experience in program management, product development, or relevant combination in diagnostics, medical devices, biotechnology, clinical laboratories, or life sciences
- Significant experience leading complex, cross-functional product development programs in a regulated environment
- Deep practical understanding of ISO 13485, IEC 62304, design controls, and medical device/IVD development processes
- Experience leading teams through design reviews, phase exits, development milestones, and regulatory readiness activities
- Hands-on experience with product development documentation, including DDPs, DHF documentation, change orders, requirements, risk documentation, and design review materials
- Experience supporting regulatory submissions such as IDE, IVDR, 510(k), PMA, or equivalent
Nice to have
- Experience supporting clinical trial execution and readiness through FPI preferred
- Experience with assay, software, and systems development; NGS diagnostics and/or MRD experience strongly preferred
- PMP certification or equivalent preferred
What you get
- Comprehensive health benefits (medical, dental, vision)
- 401(k) with company match
- Generous paid time off and company holidays
- Additional wellness and work-life benefits
- Free testing for employees and their immediate families
- Pregnancy and baby bonding leave
Worth weighing
- Remote work option available, but on-site work in Boulder, CO is also an option
- The role requires a hands-on approach, which may not suit all candidates
- The position operates in a highly regulated environment, which may involve significant compliance responsibilities
Summarised from Natera's posting. Read the full original.
Listed by Natera on their greenhouse job board, last confirmed open on 2026-09-27. PitchMeAI is not the employer.
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