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Stryker · 23 hours ago

Principal Clinical Study Manager

Irvine, California

Full-time

Hybrid

Senior Level, Lead/Staff

$118K/yr - $256K/yr

8+ years exp

Stryker is seeking a Principal Clinical Study Manager to join our Neurovascular Division. The role involves leading the planning and execution of complex clinical studies, collaborating with cross-functional teams, ensuring compliance with regulatory standards, and driving operational excellence to deliver high-quality results.

BiotechnologyHealth CareLife ScienceMedicalMedical Device

Growth Opportunities

Responsibilities

Collaborate with business unit leadership to define and manage program scope, including creating a detailed Work Breakdown Structure

Develop and maintain a comprehensive program schedule using Gantt charts; analyze critical paths, major workstreams, and intersecting milestones

Create and manage program budgets in partnership with cross-functional leaders; monitor and optimize costs to stay within budget

Partner with project teams to develop and maintain Quality Plans using industry-standard tools and techniques

Establish and execute a risk management plan, including identifying, analyzing, and mitigating program risks

Develop a Procurement Management Plan and contribute strategically to vendor selection and procurement decisions

Estimate, acquire, and allocate cross-functional resources; define roles and deliverables, provide feedback, coach team members, and support recruitment and onboarding

Create and implement stakeholder engagement and communication plans to ensure alignment across program teams, key stakeholders, and business leaders

Qualification

Program managementBudget managementCross-functional leadershipPMP certificationRisk managementStakeholder managementProcurement planningQuality systems familiarityCommunication skills