Stryker
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.
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.
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.
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.