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Senior Clinical Study Manager (Hybrid)

Stryker

Mahwah, NJHybridJob$132–220K/yrTracked 1mo agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$132–220K/yr
Location
Mahwah, NJHybrid
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Stryker is hiring a Senior Clinical Study Manager (Hybrid). Stryker is seeking a Senior Clinical Study Manager for its Joint Replacement division. This hybrid role, based in Mahwah, NJ, involves leading cross-functional projects to deliver clinical research business initiatives. The manager will drive effective project execution, stakeholder engagement, process improvement, technology implementation, and compliance-focused operational support, enhancing clinical systems and streamlining workflows.

Key focus areas include Lead cross-functional projects from initiation through implementation, stabilization, and closeout., Develop and maintain project plans, resource forecasts, communication strategies, and risk mitigation plans., and Drive implementation and optimization of clinical research technology platforms..

Successful candidates bring Bachelor's Degree In Science Or Health Care Field, 6+ Years Clinical Affairs, Clinical Operations, And/Or Clinical Project Management Experience, and Experience Leading Cross-Functional Projects Involving Business Process Transformation, Systems Implementation, Or Operational Improvement Initiatives. Important skills include Project Leadership, Stakeholder Management, Process Improvement, Technology Implementation, Compliance-Focused Operational Support, and Strategic Initiatives. Preferred (not required): Reporting, Clinical Trial Management Systems, Electronic Data Capture Systems, and Electronic Trial Master Files.

Skills & qualifications

RequiredNice to have

Skills

Project LeadershipStakeholder ManagementProcess ImprovementTechnology ImplementationCompliance-Focused Operational SupportStrategic InitiativesProject ExecutionProject ManagementResource ForecastingCommunication StrategiesRisk MitigationClinical Research Technology PlatformsRequirements GatheringTestingDeploymentTraining ActivitiesChange ManagementProcess MappingWorkflow RedesignStandardizationProject GovernanceReportingCompliant DocumentationValidationAudit ReadinessRegulatory ComplianceClinical Trial Management SystemsElectronic Data Capture SystemsElectronic Trial Master FilesElectronic Clinical Outcome Assessment ToolsAnalyticsClinical Research RegulationsISO 14155

Qualifications

Bachelor's Degree in Science or Health Care Field6+ Years Clinical Affairs, Clinical Operations, and/or Clinical Project Management ExperienceExperience Leading Cross-Functional Projects Involving Business Process Transformation, Systems Implementation, or Operational Improvement InitiativesExperience Managing Multiple Projects and Competing Priorities SimultaneouslyPMP CertificationAgile CertificationSix Sigma Certification

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

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 ISO 14155

  • Project Management Professional (PMP), Agile, Six Sigma, or comparable certification

  • US20 : $132,100 - $220,100 USD Annual

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

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.

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