Stryker
Senior Clinical Study Manager
Stryker is seeking a Senior Clinical Study Manager for our Neurovascular division. This is a hybrid position based three days per week onsite in Fremont, CA. As the Senior Clinical Study Manager, you will play a critical role in driving strategic initiatives that shape the future of healthcare innovation. This is your opportunity to lead high-visibility projects, influence outcomes, and make a difference in the lives of patients and providers around the world. What You Will Do
Responsible for day-to-day management of one or more clinical studies, to include Investigational Device Exemption (IDE), post-approval, post-market surveillance, feasibility and/or marketing studies, and/or investigator-initiated studies. Lead the development of project charters and management plans, ensuring alignment with business goals and stakeholder expectations. Own the project schedule by creating and managing detailed Gantt charts, analyzing critical paths, and tracking intersecting milestones. Define and manage project scope through collaboration with stakeholders and creation of detailed Work Breakdown Structures. Develop and maintain project budgets in partnership with cross-functional managers, ensuring costs remain within approved limits. Create and monitor project Quality Plans using multiple quality planning tools and techniques to ensure deliverables meet standards. Identify and manage project risks by developing comprehensive risk response plans and monitoring mitigation strategies. Establish procurement strategies by developing Procurement Management Plans and supporting partner selection processes. Assign and manage cross-functional resources, define roles and deliverables, and provide performance feedback to functional managers. What You Will Need
Required Bachelor's degree Minimum 6 years of clinical study management experience at the sponsor level (CRO or medical device company); site-level experience will only be considered in conjunction with sponsor Occasional travel (up to 40%) Preferred Master's degree Project Management Professional (PMP) certification or equivalent $130,700 - $215,300 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. Travel Percentage: 20% 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.
Stryker is seeking a Senior Clinical Study Manager for our Neurovascular division. This is a hybrid position based three days per week onsite in Fremont, CA. As the Senior Clinical Study Manager, you will play a critical role in driving strategic initiatives that shape the future of healthcare innovation. This is your opportunity to lead high-visibility projects, influence outcomes, and make a difference in the lives of patients and providers around the world. What You Will Do
Responsible for day-to-day management of one or more clinical studies, to include Investigational Device Exemption (IDE), post-approval, post-market surveillance, feasibility and/or marketing studies, and/or investigator-initiated studies. Lead the development of project charters and management plans, ensuring alignment with business goals and stakeholder expectations. Own the project schedule by creating and managing detailed Gantt charts, analyzing critical paths, and tracking intersecting milestones. Define and manage project scope through collaboration with stakeholders and creation of detailed Work Breakdown Structures. Develop and maintain project budgets in partnership with cross-functional managers, ensuring costs remain within approved limits. Create and monitor project Quality Plans using multiple quality planning tools and techniques to ensure deliverables meet standards. Identify and manage project risks by developing comprehensive risk response plans and monitoring mitigation strategies. Establish procurement strategies by developing Procurement Management Plans and supporting partner selection processes. Assign and manage cross-functional resources, define roles and deliverables, and provide performance feedback to functional managers. What You Will Need
Required Bachelor's degree Minimum 6 years of clinical study management experience at the sponsor level (CRO or medical device company); site-level experience will only be considered in conjunction with sponsor Occasional travel (up to 40%) Preferred Master's degree Project Management Professional (PMP) certification or equivalent $130,700 - $215,300 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. Travel Percentage: 20% 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.