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Stryker
Senior Clinical Study Manager (Hybrid)
Career Insights for Clinical Supervisor / Manager
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Based on New Jersey data
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What they do
A Clinical Supervisor or Manager supervises staff and manages services in a clinical program. May provide clinical supervision for nursing, counseling or home health care staff. Works to ensure quality patient care. Trains and develops clinical staff and manages clinical program budgets.
$119,617 / year median in New Jersey
+8% projected growth
Job Description
Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award-winning culture. We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards - not to mention various social and recreational activities, all of which are location specific. Job description We are excited to be named one of the World's Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:
US Stryker employee benefits. Stryker is hiring a Senior Clinical Study Manager for our Joint Replacement division. This is a hybrid position based in Mahwah, NJ . As Senior Clinical Study Manager, you will serve as the cross-functional project leader responsible for delivering clinical research business initiatives through effective project execution, stakeholder engagement, process improvement, technology implementation, and compliance-focused operational support. This role leads strategic initiatives that improve processes, implement technology solutions, and support operational excellence. Working with cross-functional stakeholders and external partners, you will drive projects that enhance clinical systems, streamline workflows, and strengthen business performance. What you will do Lead cross-functional projects from initiation through implementation, stabilization, and closeout, ensuring milestones, budgets, and timelines are achieved. Develop and maintain project plans, resource forecasts, communication strategies, and risk mitigation plans to support successful delivery. Drive implementation and optimization of clinical research technology platforms, coordinating requirements gathering, testing, deployment, and adoption activities. Partner with business, quality, information technology, and vendor teams to design scalable solutions that support clinical research operations. Facilitate user acceptance testing, training activities, change management initiatives, and post-implementation support. Identify opportunities to improve efficiency, quality, compliance, and user experience through process mapping, workflow redesign, and standardization efforts. Establish project governance structures and provide leadership updates, metrics, and reporting on project performance, risks, and adoption outcomes. Maintain compliant, inspection-ready documentation and support validation, audit readiness, and regulatory compliance activities throughout the project lifecycle. What you need Required Bachelor's degree in science or health care field Minimum 6 years of clinical affairs, clinical operations, and/or clinical project management experience within the device or pharmaceutical industry Experience leading cross-functional projects involving business process transformation, systems implementation, or operational improvement initiatives Experience managing multiple projects and competing priorities simultaneously Preferred Experience implementing or optimizing clinical technology platforms such as clinical trial management systems, electronic data capture systems, electronic trial master files, electronic clinical outcome assessment tools, analytics, reporting, or quality management systems Knowledge of clinical research regulations and standards, including
US Stryker employee benefits. Stryker is hiring a Senior Clinical Study Manager for our Joint Replacement division. This is a hybrid position based in Mahwah, NJ . As Senior Clinical Study Manager, you will serve as the cross-functional project leader responsible for delivering clinical research business initiatives through effective project execution, stakeholder engagement, process improvement, technology implementation, and compliance-focused operational support. This role leads strategic initiatives that improve processes, implement technology solutions, and support operational excellence. Working with cross-functional stakeholders and external partners, you will drive projects that enhance clinical systems, streamline workflows, and strengthen business performance. What you will do Lead cross-functional projects from initiation through implementation, stabilization, and closeout, ensuring milestones, budgets, and timelines are achieved. Develop and maintain project plans, resource forecasts, communication strategies, and risk mitigation plans to support successful delivery. Drive implementation and optimization of clinical research technology platforms, coordinating requirements gathering, testing, deployment, and adoption activities. Partner with business, quality, information technology, and vendor teams to design scalable solutions that support clinical research operations. Facilitate user acceptance testing, training activities, change management initiatives, and post-implementation support. Identify opportunities to improve efficiency, quality, compliance, and user experience through process mapping, workflow redesign, and standardization efforts. Establish project governance structures and provide leadership updates, metrics, and reporting on project performance, risks, and adoption outcomes. Maintain compliant, inspection-ready documentation and support validation, audit readiness, and regulatory compliance activities throughout the project lifecycle. What you need Required Bachelor's degree in science or health care field Minimum 6 years of clinical affairs, clinical operations, and/or clinical project management experience within the device or pharmaceutical industry Experience leading cross-functional projects involving business process transformation, systems implementation, or operational improvement initiatives Experience managing multiple projects and competing priorities simultaneously Preferred Experience implementing or optimizing clinical technology platforms such as clinical trial management systems, electronic data capture systems, electronic trial master files, electronic clinical outcome assessment tools, analytics, reporting, or quality management systems Knowledge of clinical research regulations and standards, including