Clinical Project Manager (Remote)
Posted 2025-08-15
Remote, USA
Full Time
Immediate Start
Stryker Neurovascular is seeking to hire a Clinical Project Manager. This role will be based on Fremont, CA or remotely anywhere in the United States.
As the Clinical Project Manager, you will focus on real world clinical evidence generation strategy, advancing medical device products that create life-changing solutions that enable people to live more active, fulfilling lives. Neurovascular | Stryker
Why come to Stryker? Dozens of Reasons To Love Stryker
Stryker will offer you a competitive total rewards package, including competitive base salary, performance bonus, and benefits. We also offer other non-financial rewards, and engaging work environment and meaningful career advancement opportunity. Stryker Benefits
WHO WE WANT:
• Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data, and insights to drive continuous improvement in functions.
• Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
WHAT YOU WILL DO:
As the Clinical Project Manager, you will be responsible for managing multiple, moderately complex clinical evidence generation studies, that are non-patient enrolling. You will focus on trial cost, schedule, and performance and on collaboration among internal and external stakeholders, decision making, and issue resolution.
· Gain input, develop, and execute on trial protocols and study project plans.
· Apply creative methodological strategies to existing data in support of targeted product goals and evidence roadmaps.
· Leverage commercial datasets and existing dataset. Familiarity with non-patient study tools and designs is preferred (survey, retrospective, meta-analysis, etc.).
· Define, manage, and own project scope.
· Develop the trial project schedule and manage through milestones.
· Create the trial budgets, and work with cross functional managers, while maintaining cost within budget.
· Monitor and maintain the project plans.
· Align key players. Develop trial communication management plan for project team and stakeholders.
· Create a risk management plan for the trial and develop a risk response plan.
WHAT YOU NEED:
• Bachelor's degree - required
• 6+ years’ experience in managing clinical trials - required
• Working knowledge of GCP, ICH guidelines, and FDA regulations - required
• Experience in protocol/report development and familiarity with various tools for data collection preferred.
This job may be performed remotely from anywhere in the United States, except that this job may not be filled or performed in Colorado. Apply tot his job
As the Clinical Project Manager, you will focus on real world clinical evidence generation strategy, advancing medical device products that create life-changing solutions that enable people to live more active, fulfilling lives. Neurovascular | Stryker
Why come to Stryker? Dozens of Reasons To Love Stryker
Stryker will offer you a competitive total rewards package, including competitive base salary, performance bonus, and benefits. We also offer other non-financial rewards, and engaging work environment and meaningful career advancement opportunity. Stryker Benefits
WHO WE WANT:
• Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data, and insights to drive continuous improvement in functions.
• Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
WHAT YOU WILL DO:
As the Clinical Project Manager, you will be responsible for managing multiple, moderately complex clinical evidence generation studies, that are non-patient enrolling. You will focus on trial cost, schedule, and performance and on collaboration among internal and external stakeholders, decision making, and issue resolution.
· Gain input, develop, and execute on trial protocols and study project plans.
· Apply creative methodological strategies to existing data in support of targeted product goals and evidence roadmaps.
· Leverage commercial datasets and existing dataset. Familiarity with non-patient study tools and designs is preferred (survey, retrospective, meta-analysis, etc.).
· Define, manage, and own project scope.
· Develop the trial project schedule and manage through milestones.
· Create the trial budgets, and work with cross functional managers, while maintaining cost within budget.
· Monitor and maintain the project plans.
· Align key players. Develop trial communication management plan for project team and stakeholders.
· Create a risk management plan for the trial and develop a risk response plan.
WHAT YOU NEED:
• Bachelor's degree - required
• 6+ years’ experience in managing clinical trials - required
• Working knowledge of GCP, ICH guidelines, and FDA regulations - required
• Experience in protocol/report development and familiarity with various tools for data collection preferred.
This job may be performed remotely from anywhere in the United States, except that this job may not be filled or performed in Colorado. Apply tot his job