
Senior Program Manager, Clinical PMO
Stryker
full-time
Posted on:
Location Type: Hybrid
Location: Fremont • California • Utah • United States
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Salary
💰 $176,300 - $293,700 per year
Job Level
Tech Stack
About the role
- Provide strategic oversight for global clinical programs, ensuring clinical trial teams execute day-to-day activities in alignment with program objectives, quality standards, and regulatory requirements.
- Lead complex, cross-functional clinical programs across feasibility, pivotal, and post-market phases, driving alignment to business strategy and timelines.
- Develop and maintain program charters, integrated schedules, and governance plans that translate clinical strategy into executable programs.
- Serve as the primary program point of contact for senior leadership, delivering clear, concise updates on progress, risks, dependencies, and recommendations.
- Partners across Regulatory, Quality, R&D, Global Supply, Finance, Sales, and Marketing to ensure clinical strategies support enterprise priorities.
- Establish, manage, and forecast annual program budgets and quarterly outlooks, ensuring financial discipline and cost efficiency.
- Proactively identify, assess, and mitigate program-level risks, escalating appropriately and driving resolution through governance forums.
- Define and monitor clinical program performance metrics, leveraging insights to drive continuous improvement and operational maturity.
- Chair program and governance meetings to ensure accountability, decision-making, and timely issue resolution.
- Lead, coach, and mentor functional managers and other direct reports, setting clear expectations, and performance objectives.
- Contribute to the advancement of the Clinical PMO by standardizing best practices, strengthening governance, and fostering a collaborative, high-performance culture.
Requirements
- Bachelor’s degree in relevant fields such as Life Sciences, Biology, Biomedical Engineering, Nursing or a related discipline.
- Minimum of 10 years of professional experience in clinical research and clinical trial development.
- 5 years minimum of leading global clinical programs across multiple phases (feasibility, pivotal, post-market).
- Required experience in Device or Pharmaceutical industry.
- Strong ability to communicate, influence, and present to senior leadership in matrixed, global organizations.
- Demonstrated experience leading complex, cross-functional programs with global scope and executive visibility.
- Experience with Good Clinical Practice (GCP).
Benefits
- Annual salary plus bonus eligible + benefits
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial developmentprogram managementrisk managementbudget forecastingperformance metricsprogram chartersgovernance plansclinical program executioncross-functional leadershipcontinuous improvement
Soft Skills
communicationinfluencepresentationcoachingmentoringcollaborationaccountabilitydecision-makingproblem-solvingstrategic oversight