What You Will Do:
Join a team where your leadership directly advances meaningful innovations that support patient care. As a Senior Project Manager within our PMO, you will drive complex, cross‑functional initiatives that shape the success of our Sage portfolio. This is an opportunity to influence outcomes, streamline execution, and partner with teams across the organization to deliver high‑impact results.
To learn more about Stryker’s Sage portfolio click here: Sage
- Lead end‑to‑end project execution by developing project charters, management plans, and ensuring delivery from initiation through completion.
- Define project scope with stakeholders and create a detailed Work Breakdown Structure to guide planning and execution.
- Develop and manage comprehensive Gantt charts; analyze critical paths and major workstreams to keep timelines on track.
- Establish and monitor sub‑project budgets in partnership with leadership, maintaining financials within approved limits.
- Create and implement risk management plans by identifying, analyzing, and addressing project risks throughout the lifecycle.
- Estimate and allocate project team resources while clarifying roles, responsibilities, and deliverables to ensure accountability.
- Build and maintain strong relationships with internal and external partners to support project outcomes and alignment.
- Apply quality system requirements consistently to ensure compliance across all project activities.
What You Will Need:
Required Qualifications:
- Bachelor of Science degree
- 6+ years of related work experience in R&D, project management, or a related field.
- Prior experience leading large and/or complex projects with cross‑functional teams
Preferred Qualifications:
- PMP or equivalent certification (e.g., PRINCE2)
- Experience working in cosmetics, formulated consumer products, or pharmaceutical/drug development environments with knowledge of regulatory and quality requirements
- Experience using project management and documentation tools such as PPM systems, Microsoft Office, SharePoint, or Visio
- Ability to produce and interpret detailed project documentation, including proposals, schedules, and objectives
Additional Information
- This role requires you to live within commuting distance of our Cary, Illinois office.
- Hybrid schedule: in the office Monday–Wednesday; work from home Thursday–Friday.
- Travel requirements: minimal travel expected.
- No relocation assistance provided
- US10: $112,900 - $188,100 USD Annual
Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
Skills Required
- Bachelor of Science degree
- 6+ years of related work experience in R&D, project management, or a related field
- Prior experience leading large and/or complex projects with cross-functional teams
- PMP or equivalent certification (e.g., PRINCE2)
- Experience working in cosmetics, formulated consumer products, or pharmaceutical/drug development environments with knowledge of regulatory and quality requirements
- Experience using project management and documentation tools such as PPM systems, Microsoft Office, SharePoint, or Visio
- Ability to produce and interpret detailed project documentation, including proposals, schedules, and objectives
- Must live within commuting distance of Cary, Illinois
Inari Medical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.
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Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
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Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
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Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.
Inari Medical Insights
What We Do
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.







