Stryker

Senior Program Manager, Clinical PMO

Stryker

full-time

Posted on:

Location Type: Hybrid

Location: FremontCaliforniaUtahUnited States

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Salary

💰 $176,300 - $293,700 per year

Job Level

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